Canonical Allele Identifier: CA153815820

Gene: UMAD1

Linked Data

• dbSNP Id: rs893362114
• gnomAD v3: 7-7739750-A-C
• gnomAD v4: 7-7739750-A-C
• MyVariant Identifiers: chr7:g.7779381A>C (hg19) ; chr7:g.7739750A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7739750A>C , CM000669.2:g.7739750A>C	GRCh38
NC_000007.13:g.7779381A>C , CM000669.1:g.7779381A>C	GRCh37
NC_000007.12:g.7745906A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682710.1:c.83-61920A>C MANE Select	ENSP00000507605.1:n.83-61920A>C
ENST00000418534.3:n.601-766T>G
ENST00000463725.5:n.323-61920A>C
ENST00000482067.3:n.174-61920A>C
ENST00000599208.1:n.436-766T>G
ENST00000628552.1:n.239-766T>G
ENST00000636849.1:c.83-61920A>C	ENSP00000489648.1:n.83-61920A>C
ENST00000638342.1:c.83-61920A>C	ENSP00000491286.1:n.83-61920A>C
ENST00000639110.1:c.83-61920A>C	ENSP00000491319.1:n.83-61920A>C
ENST00000639343.1:c.263+859A>C	ENSP00000491077.1:n.263+859A>C
NM_001302348.1:c.83-61920A>C	NP_001289277.1:n.83-61920A>C
NM_001302349.1:c.83-61920A>C	NP_001289278.1:n.83-61920A>C
NM_001302350.1:c.-23-61920A>C	NP_001289279.1:n.-23-61920A>C
XR_927014.1:n.182-766T>G
NM_001302348.2:c.83-61920A>C MANE Select	NP_001289277.1:n.83-61920A>C
NM_001302349.2:c.83-61920A>C	NP_001289278.1:n.83-61920A>C
NM_001302350.2:c.-23-61920A>C	NP_001289279.1:n.-23-61920A>C