Canonical Allele Identifier: CA339950080
Gene: ERMAP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.42830984T>G , CM000663.2:g.42830984T>G GRCh38
NC_000001.10:g.43296655T>G , CM000663.1:g.43296655T>G GRCh37
NC_000001.9:g.43069242T>G NCBI36
NG_008749.1:g.18880T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000372517.8:c.302T>G MANE Select ENSP00000361595.2:p.Val101Gly
ENST00000487556.6:n.452-4054T>G
ENST00000642150.1:n.489T>G
ENST00000647120.1:n.248-4054T>G
ENST00000328249.3:c.32T>G ENSP00000332439.3:p.Val11Gly
ENST00000372514.7:c.302T>G ENSP00000361592.3:p.Val101Gly
ENST00000372517.6:c.302T>G ENSP00000361595.2:p.Val101Gly
ENST00000487556.5:n.247-4054T>G
NM_001017922.1:c.302T>G NP_001017922.1:p.Val101Gly
NM_018538.3:c.302T>G NP_061008.2:p.Val101Gly
XM_006710313.2:c.302T>G XP_006710376.1:p.Val101Gly
XM_011540570.1:c.302T>G XP_011538872.1:p.Val101Gly
XM_011540571.1:c.302T>G XP_011538873.1:p.Val101Gly
XM_006710313.4:c.302T>G XP_006710376.1:p.Val101Gly
XM_011540570.3:c.302T>G XP_011538872.1:p.Val101Gly
XM_011540571.3:c.302T>G XP_011538873.1:p.Val101Gly
NM_001017922.2:c.302T>G MANE Select NP_001017922.1:p.Val101Gly
NM_018538.4:c.302T>G NP_061008.2:p.Val101Gly