Canonical Allele Identifier: CA802749

Gene: ERMAP

Linked Data

• dbSNP Id: rs200923604
• ExAC: 1:43296765 A / G
• gnomAD v2: 1-43296765-A-G
• gnomAD v3: 1-42831094-A-G
• gnomAD v4: 1-42831094-A-G
• MyVariant Identifiers: chr1:g.43296765A>G (hg19) ; chr1:g.42831094A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831094A>G , CM000663.2:g.42831094A>G	GRCh38
NC_000001.10:g.43296765A>G , CM000663.1:g.43296765A>G	GRCh37
NC_000001.9:g.43069352A>G	NCBI36
NG_008749.1:g.18990A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.412A>G MANE Select	ENSP00000361595.2:p.Thr138Ala
ENST00000487556.6:n.452-3944A>G
ENST00000642150.1:n.599A>G
ENST00000647120.1:n.248-3944A>G
ENST00000328249.3:c.142A>G	ENSP00000332439.3:p.Thr48Ala
ENST00000372514.7:c.412A>G	ENSP00000361592.3:p.Thr138Ala
ENST00000372517.6:c.412A>G	ENSP00000361595.2:p.Thr138Ala
ENST00000487556.5:n.247-3944A>G
NM_001017922.1:c.412A>G	NP_001017922.1:p.Thr138Ala
NM_018538.3:c.412A>G	NP_061008.2:p.Thr138Ala
XM_006710313.2:c.412A>G	XP_006710376.1:p.Thr138Ala
XM_011540570.1:c.412A>G	XP_011538872.1:p.Thr138Ala
XM_011540571.1:c.412A>G	XP_011538873.1:p.Thr138Ala
XM_006710313.4:c.412A>G	XP_006710376.1:p.Thr138Ala
XM_011540570.3:c.412A>G	XP_011538872.1:p.Thr138Ala
XM_011540571.3:c.412A>G	XP_011538873.1:p.Thr138Ala
NM_001017922.2:c.412A>G MANE Select	NP_001017922.1:p.Thr138Ala
NM_018538.4:c.412A>G	NP_061008.2:p.Thr138Ala