Canonical Allele Identifier: CA2426069139
Gene: CASK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41923065G= , CM000685.2:g.41923065G= GRCh38
NC_000023.10:g.41782318G= , CM000685.1:g.41782318G= GRCh37
NC_000023.9:g.41667262G= NCBI36
NG_016754.1:g.4970C=
NG_016754.2:g.4970C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000378154.3:c.-77C= ENSP00000367396.2:n.-77C=
ENST00000378158.6:c.-77C= ENSP00000367400.2:n.-77C=
ENST00000378163.7:c.-77C= MANE Select ENSP00000367405.1:n.-77C=
ENST00000378168.8:c.-77C= ENSP00000367410.4:n.-77C=
ENST00000442742.7:c.-77C= ENSP00000398007.3:n.-77C=
ENST00000643831.2:c.-77C= ENSP00000494388.2:n.-77C=
ENST00000644219.1:c.-77C= ENSP00000495357.1:n.-77C=
ENST00000644347.1:c.-77C= ENSP00000494183.1:n.-77C=
ENST00000645986.2:c.-77C= ENSP00000494409.2:n.-77C=
ENST00000675354.1:c.-77C= ENSP00000502315.1:n.-77C=
ENST00000378154.1:c.-77C= ENSP00000367396.1:n.-77C=
ENST00000378158.5:c.-77C= ENSP00000367400.1:n.-77C=
ENST00000378163.5:c.-77C= ENSP00000367405.1:n.-77C=
XM_005272686.3:c.-77C= XP_005272743.1:n.-77C=
XM_006724566.2:c.-77C= XP_006724629.1:n.-77C=
XM_011543993.1:c.-77C= XP_011542295.1:n.-77C=
XM_011543994.1:c.-77C= XP_011542296.1:n.-77C=
XM_011543995.1:c.-77C= XP_011542297.1:n.-77C=
XM_011543996.1:c.-77C= XP_011542298.1:n.-77C=
XM_005272686.4:c.-77C= XP_005272743.1:n.-77C=
XM_006724566.3:c.-77C= XP_006724629.1:n.-77C=
XM_011543993.2:c.-77C= XP_011542295.1:n.-77C=
XM_011543994.2:c.-77C= XP_011542296.1:n.-77C=
XM_011543995.2:c.-77C= XP_011542297.1:n.-77C=
XM_011543996.2:c.-77C= XP_011542298.1:n.-77C=
NM_001367721.1:c.-77C= MANE Select NP_001354650.1:n.-77C=