Canonical Allele Identifier: CA481434809

Gene: HAL

Linked Data

• MyVariant Identifiers: chr12:g.96384177A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.95990399A>T , CM000674.2:g.95990399A>T	GRCh38
NC_000012.11:g.96384177A>T , CM000674.1:g.96384177A>T	GRCh37
NC_000012.10:g.94908308A>T	NCBI36
NG_008180.1:g.10895T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261208.8:c.849T>A MANE Select	ENSP00000261208.3:p.Ala283=
ENST00000261208.7:c.849T>A	ENSP00000261208.3:p.Ala283=
ENST00000538703.5:c.849T>A	ENSP00000440861.1:p.Ala283=
ENST00000541929.5:c.225T>A	ENSP00000446364.1:p.Ala75=
ENST00000544080.6:c.*278T>A	ENSP00000439385.2:n.*278T>A
ENST00000546999.5:c.*278T>A	ENSP00000447675.1:n.*278T>A
ENST00000549376.1:n.242T>A
ENST00000551562.1:n.109T>A
ENST00000552509.5:c.813T>A	ENSP00000450372.1:p.Ala271=
NM_001258333.1:c.225T>A	NP_001245262.1:p.Ala75=
NM_001258334.1:c.849T>A	NP_001245263.1:p.Ala283=
NM_002108.3:c.849T>A	NP_002099.1:p.Ala283=
XM_011538249.1:c.4-2159T>A	XP_011536551.1:n.4-2159T>A
XM_011538249.2:c.4-2159T>A	XP_011536551.1:n.4-2159T>A
NM_002108.4:c.849T>A MANE Select	NP_002099.1:p.Ala283=
NM_001258334.2:c.849T>A	NP_001245263.1:p.Ala283=
NM_001258333.2:c.225T>A	NP_001245262.1:p.Ala75=