Canonical Allele Identifier: CA153830353

Gene: UMAD1

Linked Data

• dbSNP Id: rs373779585
• gnomAD v3: 7-7809494-G-A
• gnomAD v4: 7-7809494-G-A
• MyVariant Identifiers: chr7:g.7849125G>A (hg19) ; chr7:g.7809494G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7809494G>A , CM000669.2:g.7809494G>A	GRCh38
NC_000007.13:g.7849125G>A , CM000669.1:g.7849125G>A	GRCh37
NC_000007.12:g.7815650G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682710.1:c.156+7751G>A MANE Select	ENSP00000507605.1:n.156+7751G>A
ENST00000406829.2:n.168+7751G>A
ENST00000463725.5:n.396+7751G>A
ENST00000482067.3:n.247+7751G>A
ENST00000636849.1:c.156+7751G>A	ENSP00000489648.1:n.156+7751G>A
ENST00000638342.1:c.156+7751G>A	ENSP00000491286.1:n.156+7751G>A
ENST00000639110.1:c.156+7751G>A	ENSP00000491319.1:n.156+7751G>A
ENST00000639343.1:c.*58+7751G>A	ENSP00000491077.1:n.*58+7751G>A
NM_001302348.1:c.156+7751G>A	NP_001289277.1:n.156+7751G>A
NM_001302349.1:c.156+7751G>A	NP_001289278.1:n.156+7751G>A
NM_001302350.1:c.51+7751G>A	NP_001289279.1:n.51+7751G>A
NM_001302348.2:c.156+7751G>A MANE Select	NP_001289277.1:n.156+7751G>A
NM_001302349.2:c.156+7751G>A	NP_001289278.1:n.156+7751G>A
NM_001302350.2:c.51+7751G>A	NP_001289279.1:n.51+7751G>A