Canonical Allele Identifier: CA2820598121
Gene: CASK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.41853230_41853231insAAA , CM000685.2:g.41853230_41853231insAAA GRCh38
NC_000023.10:g.41712483_41712484insAAA , CM000685.1:g.41712483_41712484insAAA GRCh37
NC_000023.9:g.41597427_41597428insAAA NCBI36
NG_016754.1:g.74805_74806insTTT
NG_016754.2:g.74805_74806insTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000378154.3:c.60-3_60-2insTTT ENSP00000367396.2:n.60-3_60-2insTTT
ENST00000378158.6:c.60-3_60-2insTTT ENSP00000367400.2:n.60-3_60-2insTTT
ENST00000378163.7:c.60-3_60-2insTTT MANE Select ENSP00000367405.1:n.60-3_60-2insTTT
ENST00000378166.9:c.60-3_60-2insTTT ENSP00000367408.5:n.60-3_60-2insTTT
ENST00000378168.8:c.60-3_60-2insTTT ENSP00000367410.4:n.60-3_60-2insTTT
ENST00000421587.8:c.60-3_60-2insTTT ENSP00000400526.4:n.60-3_60-2insTTT
ENST00000442742.7:c.60-3_60-2insTTT ENSP00000398007.3:n.60-3_60-2insTTT
ENST00000468986.7:n.19-3_19-2insTTT
ENST00000643831.2:c.60-3_60-2insTTT ENSP00000494388.2:n.60-3_60-2insTTT
ENST00000644219.1:c.60-3_60-2insTTT ENSP00000495357.1:n.60-3_60-2insTTT
ENST00000644347.1:c.60-3_60-2insTTT ENSP00000494183.1:n.60-3_60-2insTTT
ENST00000644770.1:c.60-3_60-2insTTT ENSP00000494144.1:n.60-3_60-2insTTT
ENST00000645566.1:c.60-3_60-2insTTT ENSP00000494788.1:n.60-3_60-2insTTT
ENST00000645986.2:c.60-3_60-2insTTT ENSP00000494409.2:n.60-3_60-2insTTT
ENST00000646120.2:c.60-3_60-2insTTT ENSP00000495291.2:n.60-3_60-2insTTT
ENST00000647118.2:c.60-3_60-2insTTT ENSP00000493700.1:n.60-3_60-2insTTT
ENST00000675354.1:c.60-3_60-2insTTT ENSP00000502315.1:n.60-3_60-2insTTT
ENST00000378154.1:c.60-3_60-2insTTT ENSP00000367396.1:n.60-3_60-2insTTT
ENST00000378158.5:c.60-3_60-2insTTT ENSP00000367400.1:n.60-3_60-2insTTT
ENST00000378163.5:c.60-3_60-2insTTT ENSP00000367405.1:n.60-3_60-2insTTT
ENST00000378166.8:c.60-3_60-2insTTT ENSP00000367408.4:n.60-3_60-2insTTT
ENST00000421587.6:c.60-3_60-2insTTT ENSP00000400526.2:n.60-3_60-2insTTT
ENST00000442742.6:c.60-3_60-2insTTT ENSP00000398007.2:n.60-3_60-2insTTT
ENST00000468986.6:n.87-3_87-2insTTT
ENST00000477823.1:n.54-3_54-2insTTT
NM_001126054.2:c.60-3_60-2insTTT NP_001119526.1:n.60-3_60-2insTTT
NM_001126055.2:c.60-3_60-2insTTT NP_001119527.1:n.60-3_60-2insTTT
NM_003688.3:c.60-3_60-2insTTT NP_003679.2:n.60-3_60-2insTTT
XM_005272686.3:c.60-3_60-2insTTT XP_005272743.1:n.60-3_60-2insTTT
XM_006724566.2:c.60-3_60-2insTTT XP_006724629.1:n.60-3_60-2insTTT
XM_011543993.1:c.60-3_60-2insTTT XP_011542295.1:n.60-3_60-2insTTT
XM_011543994.1:c.60-3_60-2insTTT XP_011542296.1:n.60-3_60-2insTTT
XM_011543995.1:c.60-3_60-2insTTT XP_011542297.1:n.60-3_60-2insTTT
XM_011543996.1:c.60-3_60-2insTTT XP_011542298.1:n.60-3_60-2insTTT
XM_005272686.4:c.60-3_60-2insTTT XP_005272743.1:n.60-3_60-2insTTT
XM_006724566.3:c.60-3_60-2insTTT XP_006724629.1:n.60-3_60-2insTTT
XM_011543993.2:c.60-3_60-2insTTT XP_011542295.1:n.60-3_60-2insTTT
XM_011543994.2:c.60-3_60-2insTTT XP_011542296.1:n.60-3_60-2insTTT
XM_011543995.2:c.60-3_60-2insTTT XP_011542297.1:n.60-3_60-2insTTT
XM_011543996.2:c.60-3_60-2insTTT XP_011542298.1:n.60-3_60-2insTTT
NM_001367721.1:c.60-3_60-2insTTT MANE Select NP_001354650.1:n.60-3_60-2insTTT