Canonical Allele Identifier: CA1098142079

Gene: UMAD1

Linked Data

• dbSNP Id: rs1782978960
• gnomAD v3: 7-7809209-TTTG-T
• gnomAD v4: 7-7809209-TTTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.7809212_7809214del , CM000669.2:g.7809212_7809214del	GRCh38
NC_000007.13:g.7848843_7848845del , CM000669.1:g.7848843_7848845del	GRCh37
NC_000007.12:g.7815368_7815370del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000682710.1:c.156+7469_156+7471del MANE Select	ENSP00000507605.1:n.156+7469_156+7471del
ENST00000406829.2:n.168+7469_168+7471del
ENST00000463725.5:n.396+7469_396+7471del
ENST00000482067.3:n.247+7469_247+7471del
ENST00000636849.1:c.156+7469_156+7471del	ENSP00000489648.1:n.156+7469_156+7471del
ENST00000638342.1:c.156+7469_156+7471del	ENSP00000491286.1:n.156+7469_156+7471del
ENST00000639110.1:c.156+7469_156+7471del	ENSP00000491319.1:n.156+7469_156+7471del
ENST00000639343.1:c.*58+7469_*58+7471del	ENSP00000491077.1:n.*58+7469_*58+7471del
NM_001302348.1:c.156+7469_156+7471del	NP_001289277.1:n.156+7469_156+7471del
NM_001302349.1:c.156+7469_156+7471del	NP_001289278.1:n.156+7469_156+7471del
NM_001302350.1:c.51+7469_51+7471del	NP_001289279.1:n.51+7469_51+7471del
NM_001302348.2:c.156+7469_156+7471del MANE Select	NP_001289277.1:n.156+7469_156+7471del
NM_001302349.2:c.156+7469_156+7471del	NP_001289278.1:n.156+7469_156+7471del
NM_001302350.2:c.51+7469_51+7471del	NP_001289279.1:n.51+7469_51+7471del