Canonical Allele Identifier: CA1355661303

Gene: CMTM8

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.32336779G= , CM000665.2:g.32336779G=	GRCh38
NC_000003.11:g.32378271G= , CM000665.1:g.32378271G=	GRCh37
NC_000003.10:g.32353275G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307526.4:c.148-20594G= MANE Select	ENSP00000307741.3:n.148-20594G=
ENST00000307526.3:c.148-20594G=	ENSP00000307741.3:n.148-20594G=
ENST00000458535.6:c.148-31093G=	ENSP00000412934.2:n.148-31093G=
NM_178868.3:c.148-20594G=	NP_849199.2:n.148-20594G=
XM_011533416.1:c.217-20594G=	XP_011531718.1:n.217-20594G=
XM_011533417.1:c.148-31093G=	XP_011531719.1:n.148-31093G=
NM_001320308.1:c.148-31093G=	NP_001307237.1:n.148-31093G=
NM_178868.4:c.148-20594G=	NP_849199.2:n.148-20594G=
XM_011533416.3:c.217-20594G=	XP_011531718.1:n.217-20594G=
XM_017005779.1:c.19-20594G=	XP_016861268.1:n.19-20594G=
XM_017005780.1:c.-73+1855G=	XP_016861269.1:n.-73+1855G=
NM_178868.5:c.148-20594G= MANE Select	NP_849199.2:n.148-20594G=
NM_001320308.2:c.148-31093G=	NP_001307237.1:n.148-31093G=