Canonical Allele Identifier: CA358783701

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178360792G>T (hg19) ; chr4:g.177439638G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177439638G>T , CM000666.2:g.177439638G>T	GRCh38
NC_000004.11:g.178360792G>T , CM000666.1:g.178360792G>T	GRCh37
NC_000004.10:g.178597786G>T	NCBI36
NG_011845.2:g.7866C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.332C>A MANE Select	ENSP00000264595.2:p.Ala111Asp
ENST00000264595.6:c.332C>A	ENSP00000264595.2:p.Ala111Asp
ENST00000506853.5:n.366C>A
ENST00000510635.1:c.28C>A
ENST00000510955.5:n.315+635C>A
NM_000027.3:c.332C>A	NP_000018.2:p.Ala111Asp
NM_001171988.1:c.332C>A	NP_001165459.1:p.Ala111Asp
NR_033655.1:n.460C>A
XM_006714123.2:c.332C>A	XP_006714186.1:p.Ala111Asp
XR_001741155.2:n.426C>A
NM_000027.4:c.332C>A MANE Select	NP_000018.2:p.Ala111Asp
NM_001171988.2:c.332C>A	NP_001165459.1:p.Ala111Asp
NR_033655.2:n.394C>A