Canonical Allele Identifier: CA2056507415

Gene: HAL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990462A= , CM000674.2:g.95990462A=	GRCh38
NC_000012.11:g.96384240A= , CM000674.1:g.96384240A=	GRCh37
NC_000012.10:g.94908371A=	NCBI36
NG_008180.1:g.10832T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.786T= MANE Select	ENSP00000261208.3:p.His262=
ENST00000261208.7:c.786T=	ENSP00000261208.3:p.His262=
ENST00000538703.5:c.786T=	ENSP00000440861.1:p.His262=
ENST00000541929.5:c.162T=	ENSP00000446364.1:p.His54=
ENST00000544080.6:c.*215T=	ENSP00000439385.2:n.*215T=
ENST00000546999.5:c.*215T=	ENSP00000447675.1:n.*215T=
ENST00000549376.1:n.179T=
ENST00000551562.1:n.46T=
ENST00000552509.5:c.750T=	ENSP00000450372.1:p.His250=
NM_001258333.1:c.162T=	NP_001245262.1:p.His54=
NM_001258334.1:c.786T=	NP_001245263.1:p.His262=
NM_002108.3:c.786T=	NP_002099.1:p.His262=
XM_011538249.1:c.3+2218T=	XP_011536551.1:n.3+2218T=
XM_011538249.2:c.3+2218T=	XP_011536551.1:n.3+2218T=
NM_002108.4:c.786T= MANE Select	NP_002099.1:p.His262=
NM_001258334.2:c.786T=	NP_001245263.1:p.His262=
NM_001258333.2:c.162T=	NP_001245262.1:p.His54=