Canonical Allele Identifier: CA339950870

Gene: ERMAP

Linked Data

• COSMIC: COSM3489766
• MyVariant Identifiers: chr1:g.43296766C>T (hg19) ; chr1:g.42831095C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831095C>T , CM000663.2:g.42831095C>T	GRCh38
NC_000001.10:g.43296766C>T , CM000663.1:g.43296766C>T	GRCh37
NC_000001.9:g.43069353C>T	NCBI36
NG_008749.1:g.18991C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.413C>T MANE Select	ENSP00000361595.2:p.Thr138Ile
ENST00000487556.6:n.452-3943C>T
ENST00000642150.1:n.600C>T
ENST00000647120.1:n.248-3943C>T
ENST00000328249.3:c.143C>T	ENSP00000332439.3:p.Thr48Ile
ENST00000372514.7:c.413C>T	ENSP00000361592.3:p.Thr138Ile
ENST00000372517.6:c.413C>T	ENSP00000361595.2:p.Thr138Ile
ENST00000487556.5:n.247-3943C>T
NM_001017922.1:c.413C>T	NP_001017922.1:p.Thr138Ile
NM_018538.3:c.413C>T	NP_061008.2:p.Thr138Ile
XM_006710313.2:c.413C>T	XP_006710376.1:p.Thr138Ile
XM_011540570.1:c.413C>T	XP_011538872.1:p.Thr138Ile
XM_011540571.1:c.413C>T	XP_011538873.1:p.Thr138Ile
XM_006710313.4:c.413C>T	XP_006710376.1:p.Thr138Ile
XM_011540570.3:c.413C>T	XP_011538872.1:p.Thr138Ile
XM_011540571.3:c.413C>T	XP_011538873.1:p.Thr138Ile
NM_001017922.2:c.413C>T MANE Select	NP_001017922.1:p.Thr138Ile
NM_018538.4:c.413C>T	NP_061008.2:p.Thr138Ile