Canonical Allele Identifier: CA412989930

Gene: CASK

Linked Data

• MyVariant Identifiers: chrX:g.41390267T>A (hg19) ; chrX:g.41531014T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41531014T>A , CM000685.2:g.41531014T>A	GRCh38
NC_000023.10:g.41390267T>A , CM000685.1:g.41390267T>A	GRCh37
NC_000023.9:g.41275211T>A	NCBI36
NG_016754.1:g.397021A>T
NG_016754.2:g.397021A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378154.3:c.2462A>T	ENSP00000367396.2:p.Glu821Val
ENST00000378158.6:c.2459A>T	ENSP00000367400.2:p.Glu820Val
ENST00000378163.7:c.2513A>T MANE Select	ENSP00000367405.1:p.Glu838Val
ENST00000378166.9:c.2411A>T	ENSP00000367408.5:p.Glu804Val
ENST00000378168.8:c.2516A>T	ENSP00000367410.4:p.Glu839Val
ENST00000378179.9:c.1133A>T	ENSP00000367421.4:p.Glu378Val
ENST00000421587.8:c.2444A>T	ENSP00000400526.4:p.Glu815Val
ENST00000442742.7:c.2375A>T	ENSP00000398007.3:p.Glu792Val
ENST00000642499.1:n.1292A>T
ENST00000643733.1:c.285A>T
ENST00000644219.1:c.2495A>T	ENSP00000495357.1:p.Glu832Val
ENST00000644347.1:c.2426A>T	ENSP00000494183.1:p.Glu809Val
ENST00000645566.1:c.2498A>T	ENSP00000494788.1:p.Glu833Val
ENST00000645937.2:n.2744A>T
ENST00000645986.2:c.2480A>T	ENSP00000494409.2:p.Glu827Val
ENST00000646087.2:c.1835A>T	ENSP00000495510.2:p.Glu612Val
ENST00000646120.2:c.2429A>T	ENSP00000495291.2:p.Glu810Val
ENST00000675354.1:c.2447A>T	ENSP00000502315.1:p.Glu816Val
ENST00000378158.5:c.2462A>T	ENSP00000367400.1:p.Glu821Val
ENST00000378163.5:c.2513A>T	ENSP00000367405.1:p.Glu838Val
ENST00000378166.8:c.2498A>T	ENSP00000367408.4:p.Glu833Val
ENST00000378168.6:c.878A>T	ENSP00000367410.2:p.Glu293Val
ENST00000378179.7:c.1289A>T	ENSP00000367421.3:p.Glu430Val
ENST00000421587.6:c.2426A>T	ENSP00000400526.2:p.Glu809Val
ENST00000442742.6:c.2429A>T	ENSP00000398007.2:p.Glu810Val
NM_001126054.2:c.2429A>T	NP_001119526.1:p.Glu810Val
NM_001126055.2:c.2426A>T	NP_001119527.1:p.Glu809Val
NM_003688.3:c.2498A>T	NP_003679.2:p.Glu833Val
XM_005272686.3:c.2495A>T	XP_005272743.1:p.Glu832Val
XM_006724566.2:c.2390A>T	XP_006724629.1:p.Glu797Val
XM_011543993.1:c.2513A>T	XP_011542295.1:p.Glu838Val
XM_011543994.1:c.2477A>T	XP_011542296.1:p.Glu826Val
XM_011543995.1:c.2444A>T	XP_011542297.1:p.Glu815Val
XM_011543996.1:c.2408A>T	XP_011542298.1:p.Glu803Val
XM_011543997.1:c.1940A>T	XP_011542299.1:p.Glu647Val
XM_005272686.4:c.2495A>T	XP_005272743.1:p.Glu832Val
XM_006724566.3:c.2390A>T	XP_006724629.1:p.Glu797Val
XM_011543993.2:c.2513A>T	XP_011542295.1:p.Glu838Val
XM_011543994.2:c.2477A>T	XP_011542296.1:p.Glu826Val
XM_011543995.2:c.2444A>T	XP_011542297.1:p.Glu815Val
XM_011543996.2:c.2408A>T	XP_011542298.1:p.Glu803Val
XM_011543997.3:c.1940A>T	XP_011542299.1:p.Glu647Val
XM_024452473.1:c.1835A>T	XP_024308241.1:p.Glu612Val
NM_001367721.1:c.2513A>T MANE Select	NP_001354650.1:p.Glu838Val