Canonical Allele Identifier: CA412996495

Gene: CASK

Linked Data

• MyVariant Identifiers: chrX:g.41519732C>A (hg19) ; chrX:g.41660479C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41660479C>A , CM000685.2:g.41660479C>A	GRCh38
NC_000023.10:g.41519732C>A , CM000685.1:g.41519732C>A	GRCh37
NC_000023.9:g.41404676C>A	NCBI36
NG_016754.1:g.267556G>T
NG_016754.2:g.267556G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378154.3:c.791G>T	ENSP00000367396.2:p.Arg264Met
ENST00000378158.6:c.791G>T	ENSP00000367400.2:p.Arg264Met
ENST00000378163.7:c.791G>T MANE Select	ENSP00000367405.1:p.Arg264Met
ENST00000378166.9:c.791G>T	ENSP00000367408.5:p.Arg264Met
ENST00000378168.8:c.809G>T	ENSP00000367410.4:p.Arg270Met
ENST00000421587.8:c.809G>T	ENSP00000400526.4:p.Arg270Met
ENST00000442742.7:c.791G>T	ENSP00000398007.3:p.Arg264Met
ENST00000643043.2:c.236G>T	ENSP00000493518.2:p.Arg79Met
ENST00000643831.2:c.791G>T	ENSP00000494388.2:p.Arg264Met
ENST00000643853.1:n.505G>T
ENST00000644219.1:c.791G>T	ENSP00000495357.1:p.Arg264Met
ENST00000644347.1:c.791G>T	ENSP00000494183.1:p.Arg264Met
ENST00000645566.1:c.791G>T	ENSP00000494788.1:p.Arg264Met
ENST00000645986.2:c.791G>T	ENSP00000494409.2:p.Arg264Met
ENST00000646087.2:c.236G>T	ENSP00000495510.2:p.Arg79Met
ENST00000646120.2:c.791G>T	ENSP00000495291.2:p.Arg264Met
ENST00000647118.2:c.*478G>T	ENSP00000493700.1:n.*478G>T
ENST00000675354.1:c.809G>T	ENSP00000502315.1:p.Arg270Met
ENST00000378154.1:c.791G>T	ENSP00000367396.1:p.Arg264Met
ENST00000378158.5:c.791G>T	ENSP00000367400.1:p.Arg264Met
ENST00000378163.5:c.791G>T	ENSP00000367405.1:p.Arg264Met
ENST00000378166.8:c.791G>T	ENSP00000367408.4:p.Arg264Met
ENST00000421587.6:c.791G>T	ENSP00000400526.2:p.Arg264Met
ENST00000442742.6:c.791G>T	ENSP00000398007.2:p.Arg264Met
ENST00000469265.1:n.238G>T
ENST00000486402.1:n.355G>T
NM_001126054.2:c.791G>T	NP_001119526.1:p.Arg264Met
NM_001126055.2:c.791G>T	NP_001119527.1:p.Arg264Met
NM_003688.3:c.791G>T	NP_003679.2:p.Arg264Met
XM_005272686.3:c.791G>T	XP_005272743.1:p.Arg264Met
XM_006724566.2:c.791G>T	XP_006724629.1:p.Arg264Met
XM_011543993.1:c.809G>T	XP_011542295.1:p.Arg270Met
XM_011543994.1:c.809G>T	XP_011542296.1:p.Arg270Met
XM_011543995.1:c.809G>T	XP_011542297.1:p.Arg270Met
XM_011543996.1:c.809G>T	XP_011542298.1:p.Arg270Met
XM_011543997.1:c.236G>T	XP_011542299.1:p.Arg79Met
XM_005272686.4:c.791G>T	XP_005272743.1:p.Arg264Met
XM_006724566.3:c.791G>T	XP_006724629.1:p.Arg264Met
XM_011543993.2:c.809G>T	XP_011542295.1:p.Arg270Met
XM_011543994.2:c.809G>T	XP_011542296.1:p.Arg270Met
XM_011543995.2:c.809G>T	XP_011542297.1:p.Arg270Met
XM_011543996.2:c.809G>T	XP_011542298.1:p.Arg270Met
XM_011543997.3:c.236G>T	XP_011542299.1:p.Arg79Met
XM_024452473.1:c.236G>T	XP_024308241.1:p.Arg79Met
NM_001367721.1:c.791G>T MANE Select	NP_001354650.1:p.Arg264Met