Canonical Allele Identifier: CA1686250982

Gene: UMAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7809449A= , CM000669.2:g.7809449A=	GRCh38
NC_000007.13:g.7849080A= , CM000669.1:g.7849080A=	GRCh37
NC_000007.12:g.7815605A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682710.1:c.156+7706A= MANE Select	ENSP00000507605.1:n.156+7706A=
ENST00000406829.2:n.168+7706A=
ENST00000463725.5:n.396+7706A=
ENST00000482067.3:n.247+7706A=
ENST00000636849.1:c.156+7706A=	ENSP00000489648.1:n.156+7706A=
ENST00000638342.1:c.156+7706A=	ENSP00000491286.1:n.156+7706A=
ENST00000639110.1:c.156+7706A=	ENSP00000491319.1:n.156+7706A=
ENST00000639343.1:c.*58+7706A=	ENSP00000491077.1:n.*58+7706A=
NM_001302348.1:c.156+7706A=	NP_001289277.1:n.156+7706A=
NM_001302349.1:c.156+7706A=	NP_001289278.1:n.156+7706A=
NM_001302350.1:c.51+7706A=	NP_001289279.1:n.51+7706A=
NM_001302348.2:c.156+7706A= MANE Select	NP_001289277.1:n.156+7706A=
NM_001302349.2:c.156+7706A=	NP_001289278.1:n.156+7706A=
NM_001302350.2:c.51+7706A=	NP_001289279.1:n.51+7706A=