Canonical Allele Identifier: CA358785059

Gene: AGA

Linked Data

• gnomAD v4: 4-177442287-A-C
• MyVariant Identifiers: chr4:g.178363441A>C (hg19) ; chr4:g.177442287A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442287A>C , CM000666.2:g.177442287A>C	GRCh38
NC_000004.11:g.178363441A>C , CM000666.1:g.178363441A>C	GRCh37
NC_000004.10:g.178600435A>C	NCBI36
NG_011845.2:g.5217T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.89T>G MANE Select	ENSP00000264595.2:p.Val30Gly
ENST00000264595.6:c.89T>G	ENSP00000264595.2:p.Val30Gly
ENST00000506853.5:n.123T>G
ENST00000510955.5:n.123T>G
ENST00000511231.1:n.123T>G
NM_000027.3:c.89T>G	NP_000018.2:p.Val30Gly
NM_001171988.1:c.89T>G	NP_001165459.1:p.Val30Gly
NR_033655.1:n.217T>G
XM_006714123.2:c.89T>G	XP_006714186.1:p.Val30Gly
XR_001741155.2:n.183T>G
NM_000027.4:c.89T>G MANE Select	NP_000018.2:p.Val30Gly
NM_001171988.2:c.89T>G	NP_001165459.1:p.Val30Gly
NR_033655.2:n.151T>G