Canonical Allele Identifier: CA358782199

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178355576C>A (hg19) ; chr4:g.177434422C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177434422C>A , CM000666.2:g.177434422C>A	GRCh38
NC_000004.11:g.178355576C>A , CM000666.1:g.178355576C>A	GRCh37
NC_000004.10:g.178592570C>A	NCBI36
NG_011845.2:g.13082G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.766G>T MANE Select	ENSP00000264595.2:p.Ala256Ser
ENST00000264595.6:c.766G>T	ENSP00000264595.2:p.Ala256Ser
ENST00000502310.5:c.337G>T	ENSP00000423798.1:p.Ala113Ser
ENST00000506853.5:n.724G>T
NM_000027.3:c.766G>T	NP_000018.2:p.Ala256Ser
NM_001171988.1:c.736G>T	NP_001165459.1:p.Ala246Ser
NR_033655.1:n.818G>T
XM_006714123.2:c.*60G>T	XP_006714186.1:n.*60G>T
XR_001741155.2:n.838G>T
NM_000027.4:c.766G>T MANE Select	NP_000018.2:p.Ala256Ser
NM_001171988.2:c.736G>T	NP_001165459.1:p.Ala246Ser
NR_033655.2:n.752G>T