Canonical Allele Identifier: CA412988711

Gene: CASK

Linked Data

• MyVariant Identifiers: chrX:g.41379707G>T (hg19) ; chrX:g.41520454G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41520454G>T , CM000685.2:g.41520454G>T	GRCh38
NC_000023.10:g.41379707G>T , CM000685.1:g.41379707G>T	GRCh37
NC_000023.9:g.41264651G>T	NCBI36
NG_016754.1:g.407581C>A
NG_016754.2:g.407581C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378154.3:c.2696C>A	ENSP00000367396.2:p.Ala899Asp
ENST00000378158.6:c.2693C>A	ENSP00000367400.2:p.Ala898Asp
ENST00000378163.7:c.2747C>A MANE Select	ENSP00000367405.1:p.Ala916Asp
ENST00000378166.9:c.2645C>A	ENSP00000367408.5:p.Ala882Asp
ENST00000378168.8:c.2750C>A	ENSP00000367410.4:p.Ala917Asp
ENST00000378179.9:c.1367C>A	ENSP00000367421.4:p.Ala456Asp
ENST00000421587.8:c.2678C>A	ENSP00000400526.4:p.Ala893Asp
ENST00000442742.7:c.2609C>A	ENSP00000398007.3:p.Ala870Asp
ENST00000642499.1:n.1526C>A
ENST00000642641.1:n.906C>A
ENST00000643733.1:c.546C>A
ENST00000644219.1:c.2729C>A	ENSP00000495357.1:p.Ala910Asp
ENST00000644347.1:c.2660C>A	ENSP00000494183.1:p.Ala887Asp
ENST00000645566.1:c.2732C>A	ENSP00000494788.1:p.Ala911Asp
ENST00000645937.2:n.2978C>A
ENST00000645986.2:c.2834C>A	ENSP00000494409.2:p.Ala945Asp
ENST00000646087.2:c.2069C>A	ENSP00000495510.2:p.Ala690Asp
ENST00000646120.2:c.2663C>A	ENSP00000495291.2:p.Ala888Asp
ENST00000675354.1:c.2681C>A	ENSP00000502315.1:p.Ala894Asp
ENST00000378158.5:c.2696C>A	ENSP00000367400.1:p.Ala899Asp
ENST00000378163.5:c.2747C>A	ENSP00000367405.1:p.Ala916Asp
ENST00000378166.8:c.2732C>A	ENSP00000367408.4:p.Ala911Asp
ENST00000378168.6:c.1112C>A	ENSP00000367410.2:p.Ala371Asp
ENST00000378179.7:c.1523C>A	ENSP00000367421.3:p.Ala508Asp
ENST00000421587.6:c.2660C>A	ENSP00000400526.2:p.Ala887Asp
ENST00000442742.6:c.2663C>A	ENSP00000398007.2:p.Ala888Asp
NM_001126054.2:c.2663C>A	NP_001119526.1:p.Ala888Asp
NM_001126055.2:c.2660C>A	NP_001119527.1:p.Ala887Asp
NM_003688.3:c.2732C>A	NP_003679.2:p.Ala911Asp
XM_005272686.3:c.2729C>A	XP_005272743.1:p.Ala910Asp
XM_006724566.2:c.2624C>A	XP_006724629.1:p.Ala875Asp
XM_011543993.1:c.2747C>A	XP_011542295.1:p.Ala916Asp
XM_011543994.1:c.2711C>A	XP_011542296.1:p.Ala904Asp
XM_011543995.1:c.2678C>A	XP_011542297.1:p.Ala893Asp
XM_011543996.1:c.2642C>A	XP_011542298.1:p.Ala881Asp
XM_011543997.1:c.2174C>A	XP_011542299.1:p.Ala725Asp
XM_005272686.4:c.2729C>A	XP_005272743.1:p.Ala910Asp
XM_006724566.3:c.2624C>A	XP_006724629.1:p.Ala875Asp
XM_011543993.2:c.2747C>A	XP_011542295.1:p.Ala916Asp
XM_011543994.2:c.2711C>A	XP_011542296.1:p.Ala904Asp
XM_011543995.2:c.2678C>A	XP_011542297.1:p.Ala893Asp
XM_011543996.2:c.2642C>A	XP_011542298.1:p.Ala881Asp
XM_011543997.3:c.2174C>A	XP_011542299.1:p.Ala725Asp
XM_024452473.1:c.2069C>A	XP_024308241.1:p.Ala690Asp
NM_001367721.1:c.2747C>A MANE Select	NP_001354650.1:p.Ala916Asp