Canonical Allele Identifier: CA1355639840

Gene: CMTM8

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32289194C= , CM000665.2:g.32289194C=	GRCh38
NC_000003.11:g.32330686C= , CM000665.1:g.32330686C=	GRCh37
NC_000003.10:g.32305690C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_178868.5:c.147+50075C= MANE Select	NP_849199.2:n.147+50075C=
ENST00000307526.4:c.147+50075C= MANE Select	ENSP00000307741.3:n.147+50075C=
NM_001320308.1:c.147+50075C=	NP_001307237.1:n.147+50075C=
NM_001320308.2:c.147+50075C=	NP_001307237.1:n.147+50075C=
NM_178868.3:c.147+50075C=	NP_849199.2:n.147+50075C=
NM_178868.4:c.147+50075C=	NP_849199.2:n.147+50075C=
ENST00000307526.3:c.147+50075C=	ENSP00000307741.3:n.147+50075C=
ENST00000458535.6:c.147+50075C=	ENSP00000412934.2:n.147+50075C=
XM_011533416.1:c.216+6535C=	XP_011531718.1:n.216+6535C=
XM_011533416.3:c.216+6535C=	XP_011531718.1:n.216+6535C=
XM_011533417.1:c.147+50075C=	XP_011531719.1:n.147+50075C=