Canonical Allele Identifier: CA842493308

Gene: UMAD1

Linked Data

• dbSNP Id: rs1346837468
• gnomAD v3: 7-7809306-T-G
• gnomAD v4: 7-7809306-T-G
• MyVariant Identifiers: chr7:g.7848937T>G (hg19) ; chr7:g.7809306T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7809306T>G , CM000669.2:g.7809306T>G	GRCh38
NC_000007.13:g.7848937T>G , CM000669.1:g.7848937T>G	GRCh37
NC_000007.12:g.7815462T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000682710.1:c.156+7563T>G MANE Select	ENSP00000507605.1:n.156+7563T>G
ENST00000406829.2:n.168+7563T>G
ENST00000463725.5:n.396+7563T>G
ENST00000482067.3:n.247+7563T>G
ENST00000636849.1:c.156+7563T>G	ENSP00000489648.1:n.156+7563T>G
ENST00000638342.1:c.156+7563T>G	ENSP00000491286.1:n.156+7563T>G
ENST00000639110.1:c.156+7563T>G	ENSP00000491319.1:n.156+7563T>G
ENST00000639343.1:c.*58+7563T>G	ENSP00000491077.1:n.*58+7563T>G
NM_001302348.1:c.156+7563T>G	NP_001289277.1:n.156+7563T>G
NM_001302349.1:c.156+7563T>G	NP_001289278.1:n.156+7563T>G
NM_001302350.1:c.51+7563T>G	NP_001289279.1:n.51+7563T>G
NM_001302348.2:c.156+7563T>G MANE Select	NP_001289277.1:n.156+7563T>G
NM_001302349.2:c.156+7563T>G	NP_001289278.1:n.156+7563T>G
NM_001302350.2:c.51+7563T>G	NP_001289279.1:n.51+7563T>G