Canonical Allele Identifier: CA1466851468
Gene: ENAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.70642694A= , CM000666.2:g.70642694A= GRCh38
NC_000004.11:g.71508411A= , CM000666.1:g.71508411A= GRCh37
NC_000004.10:g.71727275A= NCBI36
NG_013024.1:g.18951A=

Transcript Alleles

HGVS Amino-acid change
ENST00000396073.4:c.1268A= MANE Select ENSP00000379383.4:p.Lys423=
ENST00000396073.3:c.1268A= ENSP00000379383.3:p.Lys423=
ENST00000472903.5:n.99+4851A=
NM_031889.2:c.1268A= NP_114095.2:p.Lys423=
XM_006714056.2:c.1268A= XP_006714119.1:p.Lys423=
XM_006714056.4:c.1268A= XP_006714119.1:p.Lys423=
NM_001368133.1:c.614A= NP_001355062.1:p.Lys205=
NM_031889.3:c.1268A= MANE Select NP_114095.2:p.Lys423=