Canonical Allele Identifier: CA1686223907

Gene: UMAD1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7739713G= , CM000669.2:g.7739713G=	GRCh38
NC_000007.13:g.7779344G= , CM000669.1:g.7779344G=	GRCh37
NC_000007.12:g.7745869G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000682710.1:c.83-61957G= MANE Select	ENSP00000507605.1:n.83-61957G=
ENST00000418534.3:n.601-729C=
ENST00000463725.5:n.323-61957G=
ENST00000482067.3:n.174-61957G=
ENST00000599208.1:n.436-729C=
ENST00000628552.1:n.239-729C=
ENST00000636849.1:c.83-61957G=	ENSP00000489648.1:n.83-61957G=
ENST00000638342.1:c.83-61957G=	ENSP00000491286.1:n.83-61957G=
ENST00000639110.1:c.83-61957G=	ENSP00000491319.1:n.83-61957G=
ENST00000639343.1:c.263+822G=	ENSP00000491077.1:n.263+822G=
NM_001302348.1:c.83-61957G=	NP_001289277.1:n.83-61957G=
NM_001302349.1:c.83-61957G=	NP_001289278.1:n.83-61957G=
NM_001302350.1:c.-23-61957G=	NP_001289279.1:n.-23-61957G=
XR_927014.1:n.182-729C=
NM_001302348.2:c.83-61957G= MANE Select	NP_001289277.1:n.83-61957G=
NM_001302349.2:c.83-61957G=	NP_001289278.1:n.83-61957G=
NM_001302350.2:c.-23-61957G=	NP_001289279.1:n.-23-61957G=