Canonical Allele Identifier: CA2056500193

Gene: HAL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95980902G= , CM000674.2:g.95980902G=	GRCh38
NC_000012.11:g.96374680G= , CM000674.1:g.96374680G=	GRCh37
NC_000012.10:g.94898811G=	NCBI36
NG_008180.1:g.20392C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.1288-39C= MANE Select	ENSP00000261208.3:n.1288-39C=
ENST00000261208.7:c.1288-39C=	ENSP00000261208.3:n.1288-39C=
ENST00000538703.5:c.1288-39C=	ENSP00000440861.1:n.1288-39C=
ENST00000541929.5:c.664-39C=	ENSP00000446364.1:n.664-39C=
ENST00000544080.6:c.*717-39C=	ENSP00000439385.2:n.*717-39C=
ENST00000546999.5:c.*717-39C=	ENSP00000447675.1:n.*717-39C=
NM_001258333.1:c.664-39C=	NP_001245262.1:n.664-39C=
NM_001258334.1:c.1288-39C=	NP_001245263.1:n.1288-39C=
NM_002108.3:c.1288-39C=	NP_002099.1:n.1288-39C=
XM_011538249.1:c.436-39C=	XP_011536551.1:n.436-39C=
XM_011538249.2:c.436-39C=	XP_011536551.1:n.436-39C=
XM_017019246.1:c.358-39C=	XP_016874735.1:n.358-39C=
NM_002108.4:c.1288-39C= MANE Select	NP_002099.1:n.1288-39C=
NM_001258334.2:c.1288-39C=	NP_001245263.1:n.1288-39C=
NM_001258333.2:c.664-39C=	NP_001245262.1:n.664-39C=