Canonical Allele Identifier: CA649028882

Gene: ENAM

Linked Data

• COSMIC: COSN17491324

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.70628852_70628853insC , CM000666.2:g.70628852_70628853insC	GRCh38
NC_000004.11:g.71494569_71494570insC , CM000666.1:g.71494569_71494570insC	GRCh37
NG_013024.1:g.5109_5110insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000396073.4:c.-173_-172insC MANE Select	ENSP00000379383.4:n.-173_-172insC
ENST00000396073.3:c.-173_-172insC	ENSP00000379383.3:n.-173_-172insC
NM_031889.2:c.-173_-172insC	NP_114095.2:n.-173_-172insC
XM_006714056.4:c.-649_-648insC	XP_006714119.1:n.-649_-648insC
NM_031889.3:c.-173_-172insC MANE Select	NP_114095.2:n.-173_-172insC