Canonical Allele Identifier: CA481434826

Gene: HAL

Linked Data

• MyVariant Identifiers: chr12:g.96384213C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990435C>G , CM000674.2:g.95990435C>G	GRCh38
NC_000012.11:g.96384213C>G , CM000674.1:g.96384213C>G	GRCh37
NC_000012.10:g.94908344C>G	NCBI36
NG_008180.1:g.10859G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.813G>C MANE Select	ENSP00000261208.3:p.Gly271=
ENST00000261208.7:c.813G>C	ENSP00000261208.3:p.Gly271=
ENST00000538703.5:c.813G>C	ENSP00000440861.1:p.Gly271=
ENST00000541929.5:c.189G>C	ENSP00000446364.1:p.Gly63=
ENST00000544080.6:c.*242G>C	ENSP00000439385.2:n.*242G>C
ENST00000546999.5:c.*242G>C	ENSP00000447675.1:n.*242G>C
ENST00000549376.1:n.206G>C
ENST00000551562.1:n.73G>C
ENST00000552509.5:c.777G>C	ENSP00000450372.1:p.Gly259=
NM_001258333.1:c.189G>C	NP_001245262.1:p.Gly63=
NM_001258334.1:c.813G>C	NP_001245263.1:p.Gly271=
NM_002108.3:c.813G>C	NP_002099.1:p.Gly271=
XM_011538249.1:c.4-2195G>C	XP_011536551.1:n.4-2195G>C
XM_011538249.2:c.4-2195G>C	XP_011536551.1:n.4-2195G>C
NM_002108.4:c.813G>C MANE Select	NP_002099.1:p.Gly271=
NM_001258334.2:c.813G>C	NP_001245263.1:p.Gly271=
NM_001258333.2:c.189G>C	NP_001245262.1:p.Gly63=