Canonical Allele Identifier: CA442332289
Gene: AGA HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.178355577T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.177434423T>A , CM000666.2:g.177434423T>A GRCh38
NC_000004.11:g.178355577T>A , CM000666.1:g.178355577T>A GRCh37
NC_000004.10:g.178592571T>A NCBI36
NG_011845.2:g.13081A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264595.7:c.765A>T MANE Select ENSP00000264595.2:p.Ala255=
ENST00000264595.6:c.765A>T ENSP00000264595.2:p.Ala255=
ENST00000502310.5:c.336A>T ENSP00000423798.1:p.Ala112=
ENST00000506853.5:n.723A>T
NM_000027.3:c.765A>T NP_000018.2:p.Ala255=
NM_001171988.1:c.735A>T NP_001165459.1:p.Ala245=
NR_033655.1:n.817A>T
XM_006714123.2:c.*59A>T XP_006714186.1:n.*59A>T
XR_001741155.2:n.837A>T
NM_000027.4:c.765A>T MANE Select NP_000018.2:p.Ala255=
NM_001171988.2:c.735A>T NP_001165459.1:p.Ala245=
NR_033655.2:n.751A>T