Canonical Allele Identifier: CA442332696

Gene: AGA

Linked Data

• ClinVar Variation Id: 2008806
• ClinVar RCV Id: RCV002816685
• MyVariant Identifiers: chr4:g.178360004T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177438850T>G , CM000666.2:g.177438850T>G	GRCh38
NC_000004.11:g.178360004T>G , CM000666.1:g.178360004T>G	GRCh37
NC_000004.10:g.178596998T>G	NCBI36
NG_011845.2:g.8654A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.402A>C MANE Select	ENSP00000264595.2:p.Thr134=
ENST00000264595.6:c.402A>C	ENSP00000264595.2:p.Thr134=
ENST00000502310.5:c.57A>C	ENSP00000423798.1:p.Thr19=
ENST00000506853.5:n.436A>C
ENST00000510635.1:c.98A>C
ENST00000510955.5:n.323A>C
NM_000027.3:c.402A>C	NP_000018.2:p.Thr134=
NM_001171988.1:c.402A>C	NP_001165459.1:p.Thr134=
NR_033655.1:n.530A>C
XM_006714123.2:c.402A>C	XP_006714186.1:p.Thr134=
XR_001741155.2:n.496A>C
NM_000027.4:c.402A>C MANE Select	NP_000018.2:p.Thr134=
NM_001171988.2:c.402A>C	NP_001165459.1:p.Thr134=
NR_033655.2:n.464A>C