Canonical Allele Identifier: CA358785048

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178363434G>T (hg19) ; chr4:g.177442280G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177442280G>T , CM000666.2:g.177442280G>T	GRCh38
NC_000004.11:g.178363434G>T , CM000666.1:g.178363434G>T	GRCh37
NC_000004.10:g.178600428G>T	NCBI36
NG_011845.2:g.5224C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000264595.7:c.96C>A MANE Select	ENSP00000264595.2:p.Asn32Lys
ENST00000264595.6:c.96C>A	ENSP00000264595.2:p.Asn32Lys
ENST00000506853.5:n.130C>A
ENST00000510955.5:n.130C>A
ENST00000511231.1:n.130C>A
NM_000027.3:c.96C>A	NP_000018.2:p.Asn32Lys
NM_001171988.1:c.96C>A	NP_001165459.1:p.Asn32Lys
NR_033655.1:n.224C>A
XM_006714123.2:c.96C>A	XP_006714186.1:p.Asn32Lys
XR_001741155.2:n.190C>A
NM_000027.4:c.96C>A MANE Select	NP_000018.2:p.Asn32Lys
NM_001171988.2:c.96C>A	NP_001165459.1:p.Asn32Lys
NR_033655.2:n.158C>A