Canonical Allele Identifier: CA358782659

Gene: AGA

Linked Data

• dbSNP Id: rs1736859963
• MyVariant Identifiers: chr4:g.178358592C>A (hg19) ; chr4:g.177437438C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437438C>A , CM000666.2:g.177437438C>A	GRCh38
NC_000004.11:g.178358592C>A , CM000666.1:g.178358592C>A	GRCh37
NC_000004.10:g.178595586C>A	NCBI36
NG_011845.2:g.10066G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.589G>T MANE Select	ENSP00000264595.2:p.Glu197Ter
ENST00000264595.6:c.589G>T	ENSP00000264595.2:p.Glu197Ter
ENST00000502310.5:c.244G>T	ENSP00000423798.1:p.Glu82Ter
ENST00000506853.5:n.623G>T
ENST00000510635.1:c.285G>T
ENST00000510955.5:n.510G>T
NM_000027.3:c.589G>T	NP_000018.2:p.Glu197Ter
NM_001171988.1:c.589G>T	NP_001165459.1:p.Glu197Ter
NR_033655.1:n.717G>T
XM_006714123.2:c.589G>T	XP_006714186.1:p.Glu197Ter
XR_001741155.2:n.683G>T
NM_000027.4:c.589G>T MANE Select	NP_000018.2:p.Glu197Ter
NM_001171988.2:c.589G>T	NP_001165459.1:p.Glu197Ter
NR_033655.2:n.651G>T