Canonical Allele Identifier: CA357139870
Gene: ENAM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642594A>T , CM000666.2:g.70642594A>T GRCh38
NC_000004.11:g.71508311A>T , CM000666.1:g.71508311A>T GRCh37
NC_000004.10:g.71727175A>T NCBI36
NG_013024.1:g.18851A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1168A>T MANE Select ENSP00000379383.4:p.Asn390Tyr
ENST00000396073.3:c.1168A>T ENSP00000379383.3:p.Asn390Tyr
ENST00000472903.5:n.99+4751A>T
NM_031889.2:c.1168A>T NP_114095.2:p.Asn390Tyr
XM_006714056.2:c.1168A>T XP_006714119.1:p.Asn390Tyr
XM_006714056.4:c.1168A>T XP_006714119.1:p.Asn390Tyr
NM_001368133.1:c.514A>T NP_001355062.1:p.Asn172Tyr
NM_031889.3:c.1168A>T MANE Select NP_114095.2:p.Asn390Tyr