Canonical Allele Identifier: CA358785021

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178363423A>C (hg19) ; chr4:g.177442269A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442269A>C , CM000666.2:g.177442269A>C	GRCh38
NC_000004.11:g.178363423A>C , CM000666.1:g.178363423A>C	GRCh37
NC_000004.10:g.178600417A>C	NCBI36
NG_011845.2:g.5235T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.107T>G MANE Select	ENSP00000264595.2:p.Phe36Cys
ENST00000264595.6:c.107T>G	ENSP00000264595.2:p.Phe36Cys
ENST00000506853.5:n.141T>G
ENST00000510955.5:n.141T>G
ENST00000511231.1:n.141T>G
NM_000027.3:c.107T>G	NP_000018.2:p.Phe36Cys
NM_001171988.1:c.107T>G	NP_001165459.1:p.Phe36Cys
NR_033655.1:n.235T>G
XM_006714123.2:c.107T>G	XP_006714186.1:p.Phe36Cys
XR_001741155.2:n.201T>G
NM_000027.4:c.107T>G MANE Select	NP_000018.2:p.Phe36Cys
NM_001171988.2:c.107T>G	NP_001165459.1:p.Phe36Cys
NR_033655.2:n.169T>G