Canonical Allele Identifier: CA339950900

Gene: ERMAP

Linked Data

• COSMIC: COSM5475769
• MyVariant Identifiers: chr1:g.43296769T>C (hg19) ; chr1:g.42831098T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831098T>C , CM000663.2:g.42831098T>C	GRCh38
NC_000001.10:g.43296769T>C , CM000663.1:g.43296769T>C	GRCh37
NC_000001.9:g.43069356T>C	NCBI36
NG_008749.1:g.18994T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.416T>C MANE Select	ENSP00000361595.2:p.Val139Ala
ENST00000487556.6:n.452-3940T>C
ENST00000642150.1:n.603T>C
ENST00000647120.1:n.248-3940T>C
ENST00000328249.3:c.146T>C	ENSP00000332439.3:p.Val49Ala
ENST00000372514.7:c.416T>C	ENSP00000361592.3:p.Val139Ala
ENST00000372517.6:c.416T>C	ENSP00000361595.2:p.Val139Ala
ENST00000487556.5:n.247-3940T>C
NM_001017922.1:c.416T>C	NP_001017922.1:p.Val139Ala
NM_018538.3:c.416T>C	NP_061008.2:p.Val139Ala
XM_006710313.2:c.416T>C	XP_006710376.1:p.Val139Ala
XM_011540570.1:c.416T>C	XP_011538872.1:p.Val139Ala
XM_011540571.1:c.416T>C	XP_011538873.1:p.Val139Ala
XM_006710313.4:c.416T>C	XP_006710376.1:p.Val139Ala
XM_011540570.3:c.416T>C	XP_011538872.1:p.Val139Ala
XM_011540571.3:c.416T>C	XP_011538873.1:p.Val139Ala
NM_001017922.2:c.416T>C MANE Select	NP_001017922.1:p.Val139Ala
NM_018538.4:c.416T>C	NP_061008.2:p.Val139Ala