Canonical Allele Identifier: CA2425956542

Gene: CASK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41561361_41561362delinsCA , CM000685.2:g.41561361_41561362delinsCA	GRCh38
NC_000023.10:g.41420614_41420615delinsCA , CM000685.1:g.41420614_41420615delinsCA	GRCh37
NC_000023.9:g.41305558_41305559delinsCA	NCBI36
NG_016754.1:g.366673_366674delinsTG
NG_016754.2:g.366673_366674delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378154.3:c.1668+197_1668+198delinsTG	ENSP00000367396.2:n.1668+197_1668+198delinsTG
ENST00000378158.6:c.1650+197_1650+198delinsTG	ENSP00000367400.2:n.1650+197_1650+198delinsTG
ENST00000378163.7:c.1668+197_1668+198delinsTG MANE Select	ENSP00000367405.1:n.1668+197_1668+198delinsTG
ENST00000378166.9:c.1650+197_1650+198delinsTG	ENSP00000367408.5:n.1650+197_1650+198delinsTG
ENST00000378168.8:c.1686+197_1686+198delinsTG	ENSP00000367410.4:n.1686+197_1686+198delinsTG
ENST00000378179.9:c.357+197_357+198delinsTG	ENSP00000367421.4:n.357+197_357+198delinsTG
ENST00000421587.8:c.1668+197_1668+198delinsTG	ENSP00000400526.4:n.1668+197_1668+198delinsTG
ENST00000442742.7:c.1650+197_1650+198delinsTG	ENSP00000398007.3:n.1650+197_1650+198delinsTG
ENST00000472704.3:n.279+197_279+198delinsTG
ENST00000642584.1:n.1324+197_1324+198delinsTG
ENST00000643043.2:c.1113+197_1113+198delinsTG	ENSP00000493518.2:n.1113+197_1113+198delinsTG
ENST00000644219.1:c.1650+197_1650+198delinsTG	ENSP00000495357.1:n.1650+197_1650+198delinsTG
ENST00000644347.1:c.1650+197_1650+198delinsTG	ENSP00000494183.1:n.1650+197_1650+198delinsTG
ENST00000645566.1:c.1668+197_1668+198delinsTG	ENSP00000494788.1:n.1668+197_1668+198delinsTG
ENST00000645937.2:n.1968+197_1968+198delinsTG
ENST00000645986.2:c.1650+197_1650+198delinsTG	ENSP00000494409.2:n.1650+197_1650+198delinsTG
ENST00000646087.2:c.1095+197_1095+198delinsTG	ENSP00000495510.2:n.1095+197_1095+198delinsTG
ENST00000646120.2:c.1668+197_1668+198delinsTG	ENSP00000495291.2:n.1668+197_1668+198delinsTG
ENST00000675354.1:c.1686+197_1686+198delinsTG	ENSP00000502315.1:n.1686+197_1686+198delinsTG
ENST00000378154.1:c.1668+197_1668+198delinsTG	ENSP00000367396.1:n.1668+197_1668+198delinsTG
ENST00000378158.5:c.1668+197_1668+198delinsTG	ENSP00000367400.1:n.1668+197_1668+198delinsTG
ENST00000378163.5:c.1668+197_1668+198delinsTG	ENSP00000367405.1:n.1668+197_1668+198delinsTG
ENST00000378166.8:c.1668+197_1668+198delinsTG	ENSP00000367408.4:n.1668+197_1668+198delinsTG
ENST00000378168.6:c.69+197_69+198delinsTG	ENSP00000367410.2:n.69+197_69+198delinsTG
ENST00000378179.7:c.513+197_513+198delinsTG	ENSP00000367421.3:n.513+197_513+198delinsTG
ENST00000421587.6:c.1650+197_1650+198delinsTG	ENSP00000400526.2:n.1650+197_1650+198delinsTG
ENST00000442742.6:c.1668+197_1668+198delinsTG	ENSP00000398007.2:n.1668+197_1668+198delinsTG
ENST00000472704.1:n.279+197_279+198delinsTG
NM_001126054.2:c.1668+197_1668+198delinsTG	NP_001119526.1:n.1668+197_1668+198delinsTG
NM_001126055.2:c.1650+197_1650+198delinsTG	NP_001119527.1:n.1650+197_1650+198delinsTG
NM_003688.3:c.1668+197_1668+198delinsTG	NP_003679.2:n.1668+197_1668+198delinsTG
XM_005272686.3:c.1650+197_1650+198delinsTG	XP_005272743.1:n.1650+197_1650+198delinsTG
XM_006724566.2:c.1650+197_1650+198delinsTG	XP_006724629.1:n.1650+197_1650+198delinsTG
XM_011543993.1:c.1668+197_1668+198delinsTG	XP_011542295.1:n.1668+197_1668+198delinsTG
XM_011543994.1:c.1668+197_1668+198delinsTG	XP_011542296.1:n.1668+197_1668+198delinsTG
XM_011543995.1:c.1668+197_1668+198delinsTG	XP_011542297.1:n.1668+197_1668+198delinsTG
XM_011543996.1:c.1668+197_1668+198delinsTG	XP_011542298.1:n.1668+197_1668+198delinsTG
XM_011543997.1:c.1095+197_1095+198delinsTG	XP_011542299.1:n.1095+197_1095+198delinsTG
XM_005272686.4:c.1650+197_1650+198delinsTG	XP_005272743.1:n.1650+197_1650+198delinsTG
XM_006724566.3:c.1650+197_1650+198delinsTG	XP_006724629.1:n.1650+197_1650+198delinsTG
XM_011543993.2:c.1668+197_1668+198delinsTG	XP_011542295.1:n.1668+197_1668+198delinsTG
XM_011543994.2:c.1668+197_1668+198delinsTG	XP_011542296.1:n.1668+197_1668+198delinsTG
XM_011543995.2:c.1668+197_1668+198delinsTG	XP_011542297.1:n.1668+197_1668+198delinsTG
XM_011543996.2:c.1668+197_1668+198delinsTG	XP_011542298.1:n.1668+197_1668+198delinsTG
XM_011543997.3:c.1095+197_1095+198delinsTG	XP_011542299.1:n.1095+197_1095+198delinsTG
XM_024452473.1:c.1095+197_1095+198delinsTG	XP_024308241.1:n.1095+197_1095+198delinsTG
NM_001367721.1:c.1668+197_1668+198delinsTG MANE Select	NP_001354650.1:n.1668+197_1668+198delinsTG