Canonical Allele Identifier: CA1161506382

Gene: CSMD2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.33517447A= , CM000663.2:g.33517447A=	GRCh38
NC_000001.10:g.33983047A= , CM000663.1:g.33983047A=	GRCh37
NC_000001.9:g.33755634A=	NCBI36
NG_053181.1:g.653396T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000373381.9:c.*54-877T= MANE Select	ENSP00000362479.4:n.*54-877T=
ENST00000373388.7:c.*54-877T=	ENSP00000362486.3:n.*54-877T=
ENST00000241312.8:c.*54-877T=	ENSP00000241312.4:n.*54-877T=
ENST00000373381.8:c.*54-877T=	ENSP00000362479.4:n.*54-877T=
ENST00000373388.6:c.*54-877T=	ENSP00000362486.3:n.*54-877T=
ENST00000619121.4:c.*54-877T=	ENSP00000483463.1:n.*54-877T=
NM_001281956.1:c.*54-877T=	NP_001268885.1:n.*54-877T=
NM_052896.4:c.*54-877T=	NP_443128.2:n.*54-877T=
XM_011540572.1:c.*187T=	XP_011538874.1:n.*187T=
XM_017000185.1:c.*2071T=	XP_016855674.1:n.*2071T=
XM_017000188.1:c.*2071T=	XP_016855677.1:n.*2071T=
XM_017000190.1:c.*2071T=	XP_016855679.1:n.*2071T=
XM_024452878.1:c.*2071T=	XP_024308646.1:n.*2071T=
XR_002959290.1:n.11049-877T=
XR_002959291.1:n.10875-877T=
XR_002959296.1:n.10784-877T=
NM_001281956.2:c.*54-877T= MANE Select	NP_001268885.1:n.*54-877T=
NM_052896.5:c.*54-877T=	NP_443128.2:n.*54-877T=