Canonical Allele Identifier: CA386086534

Gene: HAL

Linked Data

• dbSNP Id: rs7297245
• MyVariant Identifiers: chr12:g.96374614C>A (hg19) ; chr12:g.95980836C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95980836C>A , CM000674.2:g.95980836C>A	GRCh38
NC_000012.11:g.96374614C>A , CM000674.1:g.96374614C>A	GRCh37
NC_000012.10:g.94898745C>A	NCBI36
NG_008180.1:g.20458G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000261208.8:c.1315G>T MANE Select	ENSP00000261208.3:p.Val439Phe
ENST00000261208.7:c.1315G>T	ENSP00000261208.3:p.Val439Phe
ENST00000538703.5:c.1315G>T	ENSP00000440861.1:p.Val439Phe
ENST00000541929.5:c.691G>T	ENSP00000446364.1:p.Val231Phe
ENST00000544080.6:c.*744G>T	ENSP00000439385.2:n.*744G>T
ENST00000546999.5:c.*744G>T	ENSP00000447675.1:n.*744G>T
NM_001258333.1:c.691G>T	NP_001245262.1:p.Val231Phe
NM_001258334.1:c.1315G>T	NP_001245263.1:p.Val439Phe
NM_002108.3:c.1315G>T	NP_002099.1:p.Val439Phe
XM_011538249.1:c.463G>T	XP_011536551.1:p.Val155Phe
XM_011538249.2:c.463G>T	XP_011536551.1:p.Val155Phe
XM_017019246.1:c.385G>T	XP_016874735.1:p.Val129Phe
NM_002108.4:c.1315G>T MANE Select	NP_002099.1:p.Val439Phe
NM_001258334.2:c.1315G>T	NP_001245263.1:p.Val439Phe
NM_001258333.2:c.691G>T	NP_001245262.1:p.Val231Phe