Canonical Allele Identifier: CA1098142065
Gene: UMAD1 HGNC NCBI

Linked Data

dbSNP Id: rs1782978390

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.7809176_7809177del , CM000669.2:g.7809176_7809177del GRCh38
NC_000007.13:g.7848807_7848808del , CM000669.1:g.7848807_7848808del GRCh37
NC_000007.12:g.7815332_7815333del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000682710.1:c.156+7433_156+7434del MANE Select ENSP00000507605.1:n.156+7433_156+7434del
ENST00000406829.2:n.168+7433_168+7434del
ENST00000463725.5:n.396+7433_396+7434del
ENST00000482067.3:n.247+7433_247+7434del
ENST00000636849.1:c.156+7433_156+7434del ENSP00000489648.1:n.156+7433_156+7434del
ENST00000638342.1:c.156+7433_156+7434del ENSP00000491286.1:n.156+7433_156+7434del
ENST00000639110.1:c.156+7433_156+7434del ENSP00000491319.1:n.156+7433_156+7434del
ENST00000639343.1:c.*58+7433_*58+7434del ENSP00000491077.1:n.*58+7433_*58+7434del
NM_001302348.1:c.156+7433_156+7434del NP_001289277.1:n.156+7433_156+7434del
NM_001302349.1:c.156+7433_156+7434del NP_001289278.1:n.156+7433_156+7434del
NM_001302350.1:c.51+7433_51+7434del NP_001289279.1:n.51+7433_51+7434del
NM_001302348.2:c.156+7433_156+7434del MANE Select NP_001289277.1:n.156+7433_156+7434del
NM_001302349.2:c.156+7433_156+7434del NP_001289278.1:n.156+7433_156+7434del
NM_001302350.2:c.51+7433_51+7434del NP_001289279.1:n.51+7433_51+7434del