Canonical Allele Identifier: CA2797071976

Gene: HAL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990617dup , CM000674.2:g.95990617dup	GRCh38
NC_000012.11:g.96384395dup , CM000674.1:g.96384395dup	GRCh37
NC_000012.10:g.94908526dup	NCBI36
NG_008180.1:g.10681dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.716-81dup MANE Select	ENSP00000261208.3:n.716-81dup
ENST00000261208.7:c.716-81dup	ENSP00000261208.3:n.716-81dup
ENST00000538703.5:c.716-81dup	ENSP00000440861.1:n.716-81dup
ENST00000541929.5:c.92-81dup	ENSP00000446364.1:n.92-81dup
ENST00000544080.6:c.*145-81dup	ENSP00000439385.2:n.*145-81dup
ENST00000546579.1:c.446-81dup	ENSP00000447543.1:n.446-81dup
ENST00000546999.5:c.*145-81dup	ENSP00000447675.1:n.*145-81dup
ENST00000549376.1:n.109-81dup
ENST00000552509.5:c.680-81dup	ENSP00000450372.1:n.680-81dup
NM_001258333.1:c.92-81dup	NP_001245262.1:n.92-81dup
NM_001258334.1:c.716-81dup	NP_001245263.1:n.716-81dup
NM_002108.3:c.716-81dup	NP_002099.1:n.716-81dup
XM_011538249.1:c.3+2067dup	XP_011536551.1:n.3+2067dup
XM_011538249.2:c.3+2067dup	XP_011536551.1:n.3+2067dup
NM_002108.4:c.716-81dup MANE Select	NP_002099.1:n.716-81dup
NM_001258334.2:c.716-81dup	NP_001245263.1:n.716-81dup
NM_001258333.2:c.92-81dup	NP_001245262.1:n.92-81dup