Canonical Allele Identifier: CA153815772

Gene: UMAD1

Linked Data

• dbSNP Id: rs1023404099
• MyVariant Identifiers: chr7:g.7739547C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7739547C>T , CM000669.2:g.7739547C>T	GRCh38
NC_000007.13:g.7779178C>T , CM000669.1:g.7779178C>T	GRCh37
NC_000007.12:g.7745703C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682710.1:c.83-62123C>T MANE Select	ENSP00000507605.1:n.83-62123C>T
ENST00000418534.3:n.601-563G>A
ENST00000463725.5:n.323-62123C>T
ENST00000482067.3:n.174-62123C>T
ENST00000599208.1:n.436-563G>A
ENST00000628552.1:n.239-563G>A
ENST00000636849.1:c.83-62123C>T	ENSP00000489648.1:n.83-62123C>T
ENST00000638342.1:c.83-62123C>T	ENSP00000491286.1:n.83-62123C>T
ENST00000639110.1:c.83-62123C>T	ENSP00000491319.1:n.83-62123C>T
ENST00000639343.1:c.263+656C>T	ENSP00000491077.1:n.263+656C>T
NM_001302348.1:c.83-62123C>T	NP_001289277.1:n.83-62123C>T
NM_001302349.1:c.83-62123C>T	NP_001289278.1:n.83-62123C>T
NM_001302350.1:c.-23-62123C>T	NP_001289279.1:n.-23-62123C>T
XR_927014.1:n.182-563G>A
NM_001302348.2:c.83-62123C>T MANE Select	NP_001289277.1:n.83-62123C>T
NM_001302349.2:c.83-62123C>T	NP_001289278.1:n.83-62123C>T
NM_001302350.2:c.-23-62123C>T	NP_001289279.1:n.-23-62123C>T