Canonical Allele Identifier: CA412990095

Gene: CASK

Linked Data

• dbSNP Id: rs2064796175
• gnomAD v3: X-41531060-T-G
• gnomAD v4: X-41531060-T-G
• MyVariant Identifiers: chrX:g.41390313T>G (hg19) ; chrX:g.41531060T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41531060T>G , CM000685.2:g.41531060T>G	GRCh38
NC_000023.10:g.41390313T>G , CM000685.1:g.41390313T>G	GRCh37
NC_000023.9:g.41275257T>G	NCBI36
NG_016754.1:g.396975A>C
NG_016754.2:g.396975A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378154.3:c.2416A>C	ENSP00000367396.2:p.Ile806Leu
ENST00000378158.6:c.2413A>C	ENSP00000367400.2:p.Ile805Leu
ENST00000378163.7:c.2467A>C MANE Select	ENSP00000367405.1:p.Ile823Leu
ENST00000378166.9:c.2365A>C	ENSP00000367408.5:p.Ile789Leu
ENST00000378168.8:c.2470A>C	ENSP00000367410.4:p.Ile824Leu
ENST00000378179.9:c.1087A>C	ENSP00000367421.4:p.Ile363Leu
ENST00000421587.8:c.2398A>C	ENSP00000400526.4:p.Ile800Leu
ENST00000442742.7:c.2329A>C	ENSP00000398007.3:p.Ile777Leu
ENST00000642499.1:n.1246A>C
ENST00000643733.1:c.239A>C
ENST00000644219.1:c.2449A>C	ENSP00000495357.1:p.Ile817Leu
ENST00000644347.1:c.2380A>C	ENSP00000494183.1:p.Ile794Leu
ENST00000645566.1:c.2452A>C	ENSP00000494788.1:p.Ile818Leu
ENST00000645937.2:n.2698A>C
ENST00000645986.2:c.2434A>C	ENSP00000494409.2:p.Ile812Leu
ENST00000646087.2:c.1789A>C	ENSP00000495510.2:p.Ile597Leu
ENST00000646120.2:c.2383A>C	ENSP00000495291.2:p.Ile795Leu
ENST00000675354.1:c.2401A>C	ENSP00000502315.1:p.Ile801Leu
ENST00000378158.5:c.2416A>C	ENSP00000367400.1:p.Ile806Leu
ENST00000378163.5:c.2467A>C	ENSP00000367405.1:p.Ile823Leu
ENST00000378166.8:c.2452A>C	ENSP00000367408.4:p.Ile818Leu
ENST00000378168.6:c.832A>C	ENSP00000367410.2:p.Ile278Leu
ENST00000378179.7:c.1243A>C	ENSP00000367421.3:p.Ile415Leu
ENST00000421587.6:c.2380A>C	ENSP00000400526.2:p.Ile794Leu
ENST00000442742.6:c.2383A>C	ENSP00000398007.2:p.Ile795Leu
NM_001126054.2:c.2383A>C	NP_001119526.1:p.Ile795Leu
NM_001126055.2:c.2380A>C	NP_001119527.1:p.Ile794Leu
NM_003688.3:c.2452A>C	NP_003679.2:p.Ile818Leu
XM_005272686.3:c.2449A>C	XP_005272743.1:p.Ile817Leu
XM_006724566.2:c.2344A>C	XP_006724629.1:p.Ile782Leu
XM_011543993.1:c.2467A>C	XP_011542295.1:p.Ile823Leu
XM_011543994.1:c.2431A>C	XP_011542296.1:p.Ile811Leu
XM_011543995.1:c.2398A>C	XP_011542297.1:p.Ile800Leu
XM_011543996.1:c.2362A>C	XP_011542298.1:p.Ile788Leu
XM_011543997.1:c.1894A>C	XP_011542299.1:p.Ile632Leu
XM_005272686.4:c.2449A>C	XP_005272743.1:p.Ile817Leu
XM_006724566.3:c.2344A>C	XP_006724629.1:p.Ile782Leu
XM_011543993.2:c.2467A>C	XP_011542295.1:p.Ile823Leu
XM_011543994.2:c.2431A>C	XP_011542296.1:p.Ile811Leu
XM_011543995.2:c.2398A>C	XP_011542297.1:p.Ile800Leu
XM_011543996.2:c.2362A>C	XP_011542298.1:p.Ile788Leu
XM_011543997.3:c.1894A>C	XP_011542299.1:p.Ile632Leu
XM_024452473.1:c.1789A>C	XP_024308241.1:p.Ile597Leu
NM_001367721.1:c.2467A>C MANE Select	NP_001354650.1:p.Ile823Leu