Canonical Allele Identifier: CA339950279

Gene: ERMAP

Linked Data

• MyVariant Identifiers: chr1:g.43296679T>C (hg19) ; chr1:g.42831008T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.42831008T>C , CM000663.2:g.42831008T>C	GRCh38
NC_000001.10:g.43296679T>C , CM000663.1:g.43296679T>C	GRCh37
NC_000001.9:g.43069266T>C	NCBI36
NG_008749.1:g.18904T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372517.8:c.326T>C MANE Select	ENSP00000361595.2:p.Val109Ala
ENST00000487556.6:n.452-4030T>C
ENST00000642150.1:n.513T>C
ENST00000647120.1:n.248-4030T>C
ENST00000328249.3:c.56T>C	ENSP00000332439.3:p.Val19Ala
ENST00000372514.7:c.326T>C	ENSP00000361592.3:p.Val109Ala
ENST00000372517.6:c.326T>C	ENSP00000361595.2:p.Val109Ala
ENST00000487556.5:n.247-4030T>C
NM_001017922.1:c.326T>C	NP_001017922.1:p.Val109Ala
NM_018538.3:c.326T>C	NP_061008.2:p.Val109Ala
XM_006710313.2:c.326T>C	XP_006710376.1:p.Val109Ala
XM_011540570.1:c.326T>C	XP_011538872.1:p.Val109Ala
XM_011540571.1:c.326T>C	XP_011538873.1:p.Val109Ala
XM_006710313.4:c.326T>C	XP_006710376.1:p.Val109Ala
XM_011540570.3:c.326T>C	XP_011538872.1:p.Val109Ala
XM_011540571.3:c.326T>C	XP_011538873.1:p.Val109Ala
NM_001017922.2:c.326T>C MANE Select	NP_001017922.1:p.Val109Ala
NM_018538.4:c.326T>C	NP_061008.2:p.Val109Ala