Canonical Allele Identifier: CA386086541

Gene: HAL

Linked Data

• MyVariant Identifiers: chr12:g.96374619T>G (hg19) ; chr12:g.95980841T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95980841T>G , CM000674.2:g.95980841T>G	GRCh38
NC_000012.11:g.96374619T>G , CM000674.1:g.96374619T>G	GRCh37
NC_000012.10:g.94898750T>G	NCBI36
NG_008180.1:g.20453A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.1310A>C MANE Select	ENSP00000261208.3:p.Glu437Ala
ENST00000261208.7:c.1310A>C	ENSP00000261208.3:p.Glu437Ala
ENST00000538703.5:c.1310A>C	ENSP00000440861.1:p.Glu437Ala
ENST00000541929.5:c.686A>C	ENSP00000446364.1:p.Glu229Ala
ENST00000544080.6:c.*739A>C	ENSP00000439385.2:n.*739A>C
ENST00000546999.5:c.*739A>C	ENSP00000447675.1:n.*739A>C
NM_001258333.1:c.686A>C	NP_001245262.1:p.Glu229Ala
NM_001258334.1:c.1310A>C	NP_001245263.1:p.Glu437Ala
NM_002108.3:c.1310A>C	NP_002099.1:p.Glu437Ala
XM_011538249.1:c.458A>C	XP_011536551.1:p.Glu153Ala
XM_011538249.2:c.458A>C	XP_011536551.1:p.Glu153Ala
XM_017019246.1:c.380A>C	XP_016874735.1:p.Glu127Ala
NM_002108.4:c.1310A>C MANE Select	NP_002099.1:p.Glu437Ala
NM_001258334.2:c.1310A>C	NP_001245263.1:p.Glu437Ala
NM_001258333.2:c.686A>C	NP_001245262.1:p.Glu229Ala