Canonical Allele Identifier: CA339950637
Gene: ERMAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42831069A>T , CM000663.2:g.42831069A>T GRCh38
NC_000001.10:g.43296740A>T , CM000663.1:g.43296740A>T GRCh37
NC_000001.9:g.43069327A>T NCBI36
NG_008749.1:g.18965A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000372517.8:c.387A>T MANE Select ENSP00000361595.2:p.Gln129His
ENST00000487556.6:n.452-3969A>T
ENST00000642150.1:n.574A>T
ENST00000647120.1:n.248-3969A>T
ENST00000328249.3:c.117A>T ENSP00000332439.3:p.Gln39His
ENST00000372514.7:c.387A>T ENSP00000361592.3:p.Gln129His
ENST00000372517.6:c.387A>T ENSP00000361595.2:p.Gln129His
ENST00000487556.5:n.247-3969A>T
NM_001017922.1:c.387A>T NP_001017922.1:p.Gln129His
NM_018538.3:c.387A>T NP_061008.2:p.Gln129His
XM_006710313.2:c.387A>T XP_006710376.1:p.Gln129His
XM_011540570.1:c.387A>T XP_011538872.1:p.Gln129His
XM_011540571.1:c.387A>T XP_011538873.1:p.Gln129His
XM_006710313.4:c.387A>T XP_006710376.1:p.Gln129His
XM_011540570.3:c.387A>T XP_011538872.1:p.Gln129His
XM_011540571.3:c.387A>T XP_011538873.1:p.Gln129His
NM_001017922.2:c.387A>T MANE Select NP_001017922.1:p.Gln129His
NM_018538.4:c.387A>T NP_061008.2:p.Gln129His