Canonical Allele Identifier: CA1165371667
Gene: ERMAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42830934G= , CM000663.2:g.42830934G= GRCh38
NC_000001.10:g.43296605G= , CM000663.1:g.43296605G= GRCh37
NC_000001.9:g.43069192G= NCBI36
NG_008749.1:g.18830G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000372517.8:c.252G= MANE Select ENSP00000361595.2:p.Lys84=
ENST00000487556.6:n.452-4104G=
ENST00000642150.1:n.439G=
ENST00000647120.1:n.248-4104G=
ENST00000328249.3:c.-19G= ENSP00000332439.3:n.-19G=
ENST00000372514.7:c.252G= ENSP00000361592.3:p.Lys84=
ENST00000372517.6:c.252G= ENSP00000361595.2:p.Lys84=
ENST00000487556.5:n.247-4104G=
NM_001017922.1:c.252G= NP_001017922.1:p.Lys84=
NM_018538.3:c.252G= NP_061008.2:p.Lys84=
XM_006710313.2:c.252G= XP_006710376.1:p.Lys84=
XM_011540570.1:c.252G= XP_011538872.1:p.Lys84=
XM_011540571.1:c.252G= XP_011538873.1:p.Lys84=
XM_006710313.4:c.252G= XP_006710376.1:p.Lys84=
XM_011540570.3:c.252G= XP_011538872.1:p.Lys84=
XM_011540571.3:c.252G= XP_011538873.1:p.Lys84=
NM_001017922.2:c.252G= MANE Select NP_001017922.1:p.Lys84=
NM_018538.4:c.252G= NP_061008.2:p.Lys84=