Canonical Allele Identifier: CA386086571

Gene: HAL

Linked Data

• gnomAD v4: 12-95980854-C-T
• MyVariant Identifiers: chr12:g.96374632C>T (hg19) ; chr12:g.95980854C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95980854C>T , CM000674.2:g.95980854C>T	GRCh38
NC_000012.11:g.96374632C>T , CM000674.1:g.96374632C>T	GRCh37
NC_000012.10:g.94898763C>T	NCBI36
NG_008180.1:g.20440G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.1297G>A MANE Select	ENSP00000261208.3:p.Ala433Thr
ENST00000261208.7:c.1297G>A	ENSP00000261208.3:p.Ala433Thr
ENST00000538703.5:c.1297G>A	ENSP00000440861.1:p.Ala433Thr
ENST00000541929.5:c.673G>A	ENSP00000446364.1:p.Ala225Thr
ENST00000544080.6:c.*726G>A	ENSP00000439385.2:n.*726G>A
ENST00000546999.5:c.*726G>A	ENSP00000447675.1:n.*726G>A
NM_001258333.1:c.673G>A	NP_001245262.1:p.Ala225Thr
NM_001258334.1:c.1297G>A	NP_001245263.1:p.Ala433Thr
NM_002108.3:c.1297G>A	NP_002099.1:p.Ala433Thr
XM_011538249.1:c.445G>A	XP_011536551.1:p.Ala149Thr
XM_011538249.2:c.445G>A	XP_011536551.1:p.Ala149Thr
XM_017019246.1:c.367G>A	XP_016874735.1:p.Ala123Thr
NM_002108.4:c.1297G>A MANE Select	NP_002099.1:p.Ala433Thr
NM_001258334.2:c.1297G>A	NP_001245263.1:p.Ala433Thr
NM_001258333.2:c.673G>A	NP_001245262.1:p.Ala225Thr