Canonical Allele Identifier: CA2056507327

Gene: HAL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990384G= , CM000674.2:g.95990384G=	GRCh38
NC_000012.11:g.96384162G= , CM000674.1:g.96384162G=	GRCh37
NC_000012.10:g.94908293G=	NCBI36
NG_008180.1:g.10910C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.855+9C= MANE Select	ENSP00000261208.3:n.855+9C=
ENST00000261208.7:c.855+9C=	ENSP00000261208.3:n.855+9C=
ENST00000538703.5:c.855+9C=	ENSP00000440861.1:n.855+9C=
ENST00000541929.5:c.231+9C=	ENSP00000446364.1:n.231+9C=
ENST00000544080.6:c.*284+9C=	ENSP00000439385.2:n.*284+9C=
ENST00000546999.5:c.*284+9C=	ENSP00000447675.1:n.*284+9C=
ENST00000549376.1:n.257C=
ENST00000551562.1:n.115+9C=
ENST00000552509.5:c.819+9C=	ENSP00000450372.1:n.819+9C=
NM_001258333.1:c.231+9C=	NP_001245262.1:n.231+9C=
NM_001258334.1:c.855+9C=	NP_001245263.1:n.855+9C=
NM_002108.3:c.855+9C=	NP_002099.1:n.855+9C=
XM_011538249.1:c.4-2144C=	XP_011536551.1:n.4-2144C=
XM_011538249.2:c.4-2144C=	XP_011536551.1:n.4-2144C=
XM_017019246.1:c.-618C=	XP_016874735.1:n.-618C=
NM_002108.4:c.855+9C= MANE Select	NP_002099.1:n.855+9C=
NM_001258334.2:c.855+9C=	NP_001245263.1:n.855+9C=
NM_001258333.2:c.231+9C=	NP_001245262.1:n.231+9C=