Canonical Allele Identifier: CA1466836009

Gene: ENAM

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.70628858_70628873delinsTTGTAGTTATTTCCAC , CM000666.2:g.70628858_70628873delinsTTGTAGTTATTTCCAC	GRCh38
NC_000004.11:g.71494575_71494590delinsTTGTAGTTATTTCCAC , CM000666.1:g.71494575_71494590delinsTTGTAGTTATTTCCAC	GRCh37
NG_013024.1:g.5115_5130delinsTTGTAGTTATTTCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396073.4:c.-167_-152delinsTTGTAGTTATTTCCAC MANE Select	ENSP00000379383.4:n.-167_-152delinsTTGTAGTTATTTCCAC
ENST00000396073.3:c.-167_-152delinsTTGTAGTTATTTCCAC	ENSP00000379383.3:n.-167_-152delinsTTGTAGTTATTTCCAC
NM_031889.2:c.-167_-152delinsTTGTAGTTATTTCCAC	NP_114095.2:n.-167_-152delinsTTGTAGTTATTTCCAC
XM_006714056.2:c.-643_-628delinsTTGTAGTTATTTCCAC	XP_006714119.1:n.-643_-628delinsTTGTAGTTATTTCCAC
XM_006714056.4:c.-643_-628delinsTTGTAGTTATTTCCAC	XP_006714119.1:n.-643_-628delinsTTGTAGTTATTTCCAC
NM_031889.3:c.-167_-152delinsTTGTAGTTATTTCCAC MANE Select	NP_114095.2:n.-167_-152delinsTTGTAGTTATTTCCAC