Canonical Allele Identifier: CA481434870

Gene: HAL

Linked Data

• MyVariant Identifiers: chr12:g.96384267G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990489G>A , CM000674.2:g.95990489G>A	GRCh38
NC_000012.11:g.96384267G>A , CM000674.1:g.96384267G>A	GRCh37
NC_000012.10:g.94908398G>A	NCBI36
NG_008180.1:g.10805C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.759C>T MANE Select	ENSP00000261208.3:p.Ala253=
ENST00000261208.7:c.759C>T	ENSP00000261208.3:p.Ala253=
ENST00000538703.5:c.759C>T	ENSP00000440861.1:p.Ala253=
ENST00000541929.5:c.135C>T	ENSP00000446364.1:p.Ala45=
ENST00000544080.6:c.*188C>T	ENSP00000439385.2:n.*188C>T
ENST00000546999.5:c.*188C>T	ENSP00000447675.1:n.*188C>T
ENST00000549376.1:n.152C>T
ENST00000551562.1:n.19C>T
ENST00000552509.5:c.723C>T	ENSP00000450372.1:p.Ala241=
NM_001258333.1:c.135C>T	NP_001245262.1:p.Ala45=
NM_001258334.1:c.759C>T	NP_001245263.1:p.Ala253=
NM_002108.3:c.759C>T	NP_002099.1:p.Ala253=
XM_011538249.1:c.3+2191C>T	XP_011536551.1:n.3+2191C>T
XM_011538249.2:c.3+2191C>T	XP_011536551.1:n.3+2191C>T
NM_002108.4:c.759C>T MANE Select	NP_002099.1:p.Ala253=
NM_001258334.2:c.759C>T	NP_001245263.1:p.Ala253=
NM_001258333.2:c.135C>T	NP_001245262.1:p.Ala45=