Canonical Allele Identifier: CA481434821

Gene: HAL

Linked Data

• MyVariant Identifiers: chr12:g.96384201A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990423A>G , CM000674.2:g.95990423A>G	GRCh38
NC_000012.11:g.96384201A>G , CM000674.1:g.96384201A>G	GRCh37
NC_000012.10:g.94908332A>G	NCBI36
NG_008180.1:g.10871T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.825T>C MANE Select	ENSP00000261208.3:p.Ser275=
ENST00000261208.7:c.825T>C	ENSP00000261208.3:p.Ser275=
ENST00000538703.5:c.825T>C	ENSP00000440861.1:p.Ser275=
ENST00000541929.5:c.201T>C	ENSP00000446364.1:p.Ser67=
ENST00000544080.6:c.*254T>C	ENSP00000439385.2:n.*254T>C
ENST00000546999.5:c.*254T>C	ENSP00000447675.1:n.*254T>C
ENST00000549376.1:n.218T>C
ENST00000551562.1:n.85T>C
ENST00000552509.5:c.789T>C	ENSP00000450372.1:p.Ser263=
NM_001258333.1:c.201T>C	NP_001245262.1:p.Ser67=
NM_001258334.1:c.825T>C	NP_001245263.1:p.Ser275=
NM_002108.3:c.825T>C	NP_002099.1:p.Ser275=
XM_011538249.1:c.4-2183T>C	XP_011536551.1:n.4-2183T>C
XM_011538249.2:c.4-2183T>C	XP_011536551.1:n.4-2183T>C
NM_002108.4:c.825T>C MANE Select	NP_002099.1:p.Ser275=
NM_001258334.2:c.825T>C	NP_001245263.1:p.Ser275=
NM_001258333.2:c.201T>C	NP_001245262.1:p.Ser67=