Canonical Allele Identifier: CA2762110796

Gene: ENAM

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.70628815A>G , CM000666.2:g.70628815A>G	GRCh38
NC_000004.11:g.71494532A>G , CM000666.1:g.71494532A>G	GRCh37
NG_013024.1:g.5072A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000396073.4:c.-210A>G MANE Select	ENSP00000379383.4:n.-210A>G
ENST00000396073.3:c.-210A>G	ENSP00000379383.3:n.-210A>G
NM_031889.2:c.-210A>G	NP_114095.2:n.-210A>G
XM_006714056.4:c.-686A>G	XP_006714119.1:n.-686A>G
NM_031889.3:c.-210A>G MANE Select	NP_114095.2:n.-210A>G