Canonical Allele Identifier: CA412989983

Gene: CASK

Linked Data

• MyVariant Identifiers: chrX:g.41390283C>A (hg19) ; chrX:g.41531030C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41531030C>A , CM000685.2:g.41531030C>A	GRCh38
NC_000023.10:g.41390283C>A , CM000685.1:g.41390283C>A	GRCh37
NC_000023.9:g.41275227C>A	NCBI36
NG_016754.1:g.397005G>T
NG_016754.2:g.397005G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378154.3:c.2446G>T	ENSP00000367396.2:p.Ala816Ser
ENST00000378158.6:c.2443G>T	ENSP00000367400.2:p.Ala815Ser
ENST00000378163.7:c.2497G>T MANE Select	ENSP00000367405.1:p.Ala833Ser
ENST00000378166.9:c.2395G>T	ENSP00000367408.5:p.Ala799Ser
ENST00000378168.8:c.2500G>T	ENSP00000367410.4:p.Ala834Ser
ENST00000378179.9:c.1117G>T	ENSP00000367421.4:p.Ala373Ser
ENST00000421587.8:c.2428G>T	ENSP00000400526.4:p.Ala810Ser
ENST00000442742.7:c.2359G>T	ENSP00000398007.3:p.Ala787Ser
ENST00000642499.1:n.1276G>T
ENST00000643733.1:c.269G>T
ENST00000644219.1:c.2479G>T	ENSP00000495357.1:p.Ala827Ser
ENST00000644347.1:c.2410G>T	ENSP00000494183.1:p.Ala804Ser
ENST00000645566.1:c.2482G>T	ENSP00000494788.1:p.Ala828Ser
ENST00000645937.2:n.2728G>T
ENST00000645986.2:c.2464G>T	ENSP00000494409.2:p.Ala822Ser
ENST00000646087.2:c.1819G>T	ENSP00000495510.2:p.Ala607Ser
ENST00000646120.2:c.2413G>T	ENSP00000495291.2:p.Ala805Ser
ENST00000675354.1:c.2431G>T	ENSP00000502315.1:p.Ala811Ser
ENST00000378158.5:c.2446G>T	ENSP00000367400.1:p.Ala816Ser
ENST00000378163.5:c.2497G>T	ENSP00000367405.1:p.Ala833Ser
ENST00000378166.8:c.2482G>T	ENSP00000367408.4:p.Ala828Ser
ENST00000378168.6:c.862G>T	ENSP00000367410.2:p.Ala288Ser
ENST00000378179.7:c.1273G>T	ENSP00000367421.3:p.Ala425Ser
ENST00000421587.6:c.2410G>T	ENSP00000400526.2:p.Ala804Ser
ENST00000442742.6:c.2413G>T	ENSP00000398007.2:p.Ala805Ser
NM_001126054.2:c.2413G>T	NP_001119526.1:p.Ala805Ser
NM_001126055.2:c.2410G>T	NP_001119527.1:p.Ala804Ser
NM_003688.3:c.2482G>T	NP_003679.2:p.Ala828Ser
XM_005272686.3:c.2479G>T	XP_005272743.1:p.Ala827Ser
XM_006724566.2:c.2374G>T	XP_006724629.1:p.Ala792Ser
XM_011543993.1:c.2497G>T	XP_011542295.1:p.Ala833Ser
XM_011543994.1:c.2461G>T	XP_011542296.1:p.Ala821Ser
XM_011543995.1:c.2428G>T	XP_011542297.1:p.Ala810Ser
XM_011543996.1:c.2392G>T	XP_011542298.1:p.Ala798Ser
XM_011543997.1:c.1924G>T	XP_011542299.1:p.Ala642Ser
XM_005272686.4:c.2479G>T	XP_005272743.1:p.Ala827Ser
XM_006724566.3:c.2374G>T	XP_006724629.1:p.Ala792Ser
XM_011543993.2:c.2497G>T	XP_011542295.1:p.Ala833Ser
XM_011543994.2:c.2461G>T	XP_011542296.1:p.Ala821Ser
XM_011543995.2:c.2428G>T	XP_011542297.1:p.Ala810Ser
XM_011543996.2:c.2392G>T	XP_011542298.1:p.Ala798Ser
XM_011543997.3:c.1924G>T	XP_011542299.1:p.Ala642Ser
XM_024452473.1:c.1819G>T	XP_024308241.1:p.Ala607Ser
NM_001367721.1:c.2497G>T MANE Select	NP_001354650.1:p.Ala833Ser