Canonical Allele Identifier: CA1686250910
Gene: UMAD1 HGNC NCBI

Linked Data

dbSNP Id: rs1782980215

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.7809293del , CM000669.2:g.7809293del GRCh38
NC_000007.13:g.7848924del , CM000669.1:g.7848924del GRCh37
NC_000007.12:g.7815449del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000682710.1:c.156+7550del MANE Select ENSP00000507605.1:n.156+7550del
ENST00000406829.2:n.168+7550del
ENST00000463725.5:n.396+7550del
ENST00000482067.3:n.247+7550del
ENST00000636849.1:c.156+7550del ENSP00000489648.1:n.156+7550del
ENST00000638342.1:c.156+7550del ENSP00000491286.1:n.156+7550del
ENST00000639110.1:c.156+7550del ENSP00000491319.1:n.156+7550del
ENST00000639343.1:c.*58+7550del ENSP00000491077.1:n.*58+7550del
NM_001302348.1:c.156+7550del NP_001289277.1:n.156+7550del
NM_001302349.1:c.156+7550del NP_001289278.1:n.156+7550del
NM_001302350.1:c.51+7550del NP_001289279.1:n.51+7550del
NM_001302348.2:c.156+7550del MANE Select NP_001289277.1:n.156+7550del
NM_001302349.2:c.156+7550del NP_001289278.1:n.156+7550del
NM_001302350.2:c.51+7550del NP_001289279.1:n.51+7550del