Canonical Allele Identifier: CA442332677

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178359965A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438811A>T , CM000666.2:g.177438811A>T	GRCh38
NC_000004.11:g.178359965A>T , CM000666.1:g.178359965A>T	GRCh37
NC_000004.10:g.178596959A>T	NCBI36
NG_011845.2:g.8693T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.441T>A MANE Select	ENSP00000264595.2:p.Ser147=
ENST00000264595.6:c.441T>A	ENSP00000264595.2:p.Ser147=
ENST00000502310.5:c.96T>A	ENSP00000423798.1:p.Ser32=
ENST00000506853.5:n.475T>A
ENST00000510635.1:c.137T>A
ENST00000510955.5:n.362T>A
NM_000027.3:c.441T>A	NP_000018.2:p.Ser147=
NM_001171988.1:c.441T>A	NP_001165459.1:p.Ser147=
NR_033655.1:n.569T>A
XM_006714123.2:c.441T>A	XP_006714186.1:p.Ser147=
XR_001741155.2:n.535T>A
NM_000027.4:c.441T>A MANE Select	NP_000018.2:p.Ser147=
NM_001171988.2:c.441T>A	NP_001165459.1:p.Ser147=
NR_033655.2:n.503T>A