Canonical Allele Identifier: CA2056507357

Gene: HAL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990404C= , CM000674.2:g.95990404C=	GRCh38
NC_000012.11:g.96384182C= , CM000674.1:g.96384182C=	GRCh37
NC_000012.10:g.94908313C=	NCBI36
NG_008180.1:g.10890G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.844G= MANE Select	ENSP00000261208.3:p.Asp282=
ENST00000261208.7:c.844G=	ENSP00000261208.3:p.Asp282=
ENST00000538703.5:c.844G=	ENSP00000440861.1:p.Asp282=
ENST00000541929.5:c.220G=	ENSP00000446364.1:p.Asp74=
ENST00000544080.6:c.*273G=	ENSP00000439385.2:n.*273G=
ENST00000546999.5:c.*273G=	ENSP00000447675.1:n.*273G=
ENST00000549376.1:n.237G=
ENST00000551562.1:n.104G=
ENST00000552509.5:c.808G=	ENSP00000450372.1:p.Asp270=
NM_001258333.1:c.220G=	NP_001245262.1:p.Asp74=
NM_001258334.1:c.844G=	NP_001245263.1:p.Asp282=
NM_002108.3:c.844G=	NP_002099.1:p.Asp282=
XM_011538249.1:c.4-2164G=	XP_011536551.1:n.4-2164G=
XM_011538249.2:c.4-2164G=	XP_011536551.1:n.4-2164G=
NM_002108.4:c.844G= MANE Select	NP_002099.1:p.Asp282=
NM_001258334.2:c.844G=	NP_001245263.1:p.Asp282=
NM_001258333.2:c.220G=	NP_001245262.1:p.Asp74=