Canonical Allele Identifier: CA516098299

Gene: CASK

Linked Data

• MyVariant Identifiers: chrX:g.41379706G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.41520453G>A , CM000685.2:g.41520453G>A	GRCh38
NC_000023.10:g.41379706G>A , CM000685.1:g.41379706G>A	GRCh37
NC_000023.9:g.41264650G>A	NCBI36
NG_016754.1:g.407582C>T
NG_016754.2:g.407582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000378154.3:c.2697C>T	ENSP00000367396.2:p.Ala899=
ENST00000378158.6:c.2694C>T	ENSP00000367400.2:p.Ala898=
ENST00000378163.7:c.2748C>T MANE Select	ENSP00000367405.1:p.Ala916=
ENST00000378166.9:c.2646C>T	ENSP00000367408.5:p.Ala882=
ENST00000378168.8:c.2751C>T	ENSP00000367410.4:p.Ala917=
ENST00000378179.9:c.1368C>T	ENSP00000367421.4:p.Ala456=
ENST00000421587.8:c.2679C>T	ENSP00000400526.4:p.Ala893=
ENST00000442742.7:c.2610C>T	ENSP00000398007.3:p.Ala870=
ENST00000642499.1:n.1527C>T
ENST00000642641.1:n.907C>T
ENST00000643733.1:c.547C>T
ENST00000644219.1:c.2730C>T	ENSP00000495357.1:p.Ala910=
ENST00000644347.1:c.2661C>T	ENSP00000494183.1:p.Ala887=
ENST00000645566.1:c.2733C>T	ENSP00000494788.1:p.Ala911=
ENST00000645937.2:n.2979C>T
ENST00000645986.2:c.2835C>T	ENSP00000494409.2:p.Ala945=
ENST00000646087.2:c.2070C>T	ENSP00000495510.2:p.Ala690=
ENST00000646120.2:c.2664C>T	ENSP00000495291.2:p.Ala888=
ENST00000675354.1:c.2682C>T	ENSP00000502315.1:p.Ala894=
ENST00000378158.5:c.2697C>T	ENSP00000367400.1:p.Ala899=
ENST00000378163.5:c.2748C>T	ENSP00000367405.1:p.Ala916=
ENST00000378166.8:c.2733C>T	ENSP00000367408.4:p.Ala911=
ENST00000378168.6:c.1113C>T	ENSP00000367410.2:p.Ala371=
ENST00000378179.7:c.1524C>T	ENSP00000367421.3:p.Ala508=
ENST00000421587.6:c.2661C>T	ENSP00000400526.2:p.Ala887=
ENST00000442742.6:c.2664C>T	ENSP00000398007.2:p.Ala888=
NM_001126054.2:c.2664C>T	NP_001119526.1:p.Ala888=
NM_001126055.2:c.2661C>T	NP_001119527.1:p.Ala887=
NM_003688.3:c.2733C>T	NP_003679.2:p.Ala911=
XM_005272686.3:c.2730C>T	XP_005272743.1:p.Ala910=
XM_006724566.2:c.2625C>T	XP_006724629.1:p.Ala875=
XM_011543993.1:c.2748C>T	XP_011542295.1:p.Ala916=
XM_011543994.1:c.2712C>T	XP_011542296.1:p.Ala904=
XM_011543995.1:c.2679C>T	XP_011542297.1:p.Ala893=
XM_011543996.1:c.2643C>T	XP_011542298.1:p.Ala881=
XM_011543997.1:c.2175C>T	XP_011542299.1:p.Ala725=
XM_005272686.4:c.2730C>T	XP_005272743.1:p.Ala910=
XM_006724566.3:c.2625C>T	XP_006724629.1:p.Ala875=
XM_011543993.2:c.2748C>T	XP_011542295.1:p.Ala916=
XM_011543994.2:c.2712C>T	XP_011542296.1:p.Ala904=
XM_011543995.2:c.2679C>T	XP_011542297.1:p.Ala893=
XM_011543996.2:c.2643C>T	XP_011542298.1:p.Ala881=
XM_011543997.3:c.2175C>T	XP_011542299.1:p.Ala725=
XM_024452473.1:c.2070C>T	XP_024308241.1:p.Ala690=
NM_001367721.1:c.2748C>T MANE Select	NP_001354650.1:p.Ala916=