Canonical Allele Identifier: CA358784336

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178361497C>A (hg19) ; chr4:g.177440343C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177440343C>A , CM000666.2:g.177440343C>A	GRCh38
NC_000004.11:g.178361497C>A , CM000666.1:g.178361497C>A	GRCh37
NC_000004.10:g.178598491C>A	NCBI36
NG_011845.2:g.7161G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.211G>T MANE Select	ENSP00000264595.2:p.Gly71Cys
ENST00000264595.6:c.211G>T	ENSP00000264595.2:p.Gly71Cys
ENST00000506853.5:n.245G>T
ENST00000510955.5:n.245G>T
ENST00000511231.1:n.245G>T
NM_000027.3:c.211G>T	NP_000018.2:p.Gly71Cys
NM_001171988.1:c.211G>T	NP_001165459.1:p.Gly71Cys
NR_033655.1:n.339G>T
XM_006714123.2:c.211G>T	XP_006714186.1:p.Gly71Cys
XR_001741155.2:n.305G>T
NM_000027.4:c.211G>T MANE Select	NP_000018.2:p.Gly71Cys
NM_001171988.2:c.211G>T	NP_001165459.1:p.Gly71Cys
NR_033655.2:n.273G>T