Canonical Allele Identifier: CA16594524
Gene: UMODL1 HGNC NCBI

Linked Data

dbSNP Id: rs1475911

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42093370A>C , CM000683.2:g.42093370A>C GRCh38
NC_000021.8:g.43513480A>C , CM000683.1:g.43513480A>C GRCh37
NC_000021.7:g.42386549A>C NCBI36
NG_055246.1:g.35412A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000408910.7:c.931+2932A>C MANE Select ENSP00000386147.2:n.931+2932A>C
ENST00000400421.6:c.438+2932A>C
ENST00000400424.6:c.715+2932A>C ENSP00000383276.1:n.715+2932A>C
ENST00000400427.5:c.715+2932A>C ENSP00000383279.1:n.715+2932A>C
ENST00000408910.6:c.931+2932A>C ENSP00000386147.2:n.931+2932A>C
ENST00000408989.6:c.931+2932A>C ENSP00000386126.2:n.931+2932A>C
ENST00000466434.5:c.439-501A>C
ENST00000468982.5:c.535+2932A>C
ENST00000485357.1:c.252-34A>C
ENST00000491559.5:c.432-34A>C
ENST00000497243.5:c.359+4890A>C
NM_001004416.2:c.931+2932A>C NP_001004416.2:n.931+2932A>C
NM_001199527.1:c.715+2932A>C NP_001186456.1:n.715+2932A>C
NM_001199528.2:c.715+2932A>C NP_001186457.2:n.715+2932A>C
NM_173568.3:c.931+2932A>C NP_775839.3:n.931+2932A>C
XM_011529787.1:c.715+2932A>C XP_011528089.1:n.715+2932A>C
XM_011529788.1:c.715+2932A>C XP_011528090.1:n.715+2932A>C
XM_011529789.1:c.715+2932A>C XP_011528091.1:n.715+2932A>C
XM_011529790.1:c.619+2932A>C XP_011528092.1:n.619+2932A>C
XM_011529791.1:c.619+2932A>C XP_011528093.1:n.619+2932A>C
XM_011529793.1:c.619+2932A>C XP_011528095.1:n.619+2932A>C
XM_011529794.1:c.619+2932A>C XP_011528096.1:n.619+2932A>C
XM_011529795.1:c.619+2932A>C XP_011528097.1:n.619+2932A>C
XM_011529796.1:c.715+2932A>C XP_011528098.1:n.715+2932A>C
XM_011529797.1:c.397+2932A>C XP_011528099.1:n.397+2932A>C
XM_011529798.1:c.397+2932A>C XP_011528100.1:n.397+2932A>C
XM_011529799.1:c.715+2932A>C XP_011528101.1:n.715+2932A>C
XM_011529800.1:c.334+2932A>C XP_011528102.1:n.334+2932A>C
XM_011529803.1:c.715+2932A>C XP_011528105.1:n.715+2932A>C
XR_937578.1:n.785+2932A>C
XR_937579.1:n.785+2932A>C
XR_937580.1:n.785+2932A>C
XM_017028506.1:c.715+2932A>C XP_016883995.1:n.715+2932A>C
XM_017028507.1:c.619+2932A>C XP_016883996.1:n.619+2932A>C
NM_001199527.2:c.715+2932A>C NP_001186456.2:n.715+2932A>C
NM_001199528.3:c.715+2932A>C NP_001186457.3:n.715+2932A>C
NM_001004416.3:c.931+2932A>C MANE Select NP_001004416.3:n.931+2932A>C
NM_001199527.3:c.715+2932A>C NP_001186456.2:n.715+2932A>C
NM_001199528.4:c.715+2932A>C NP_001186457.3:n.715+2932A>C
NM_173568.4:c.931+2932A>C NP_775839.4:n.931+2932A>C