Canonical Allele Identifier: CA110788536

Gene: AGA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177436212C>T , CM000666.2:g.177436212C>T	GRCh38
NC_000004.11:g.178357366C>T , CM000666.1:g.178357366C>T	GRCh37
NC_000004.10:g.178594360C>T	NCBI36
NG_011845.2:g.11292G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000027.4:c.698+64G>A MANE Select	NP_000018.2:n.698+64G>A
ENST00000264595.7:c.698+64G>A MANE Select	ENSP00000264595.2:n.698+64G>A
NM_000027.3:c.698+64G>A	NP_000018.2:n.698+64G>A
NM_001171988.1:c.676+86G>A	NP_001165459.1:n.676+86G>A
NM_001171988.2:c.676+86G>A	NP_001165459.1:n.676+86G>A
NR_033655.1:n.750+1193G>A
NR_033655.2:n.684+1193G>A
ENST00000264595.6:c.698+64G>A	ENSP00000264595.2:n.698+64G>A
ENST00000502310.5:c.277+1193G>A	ENSP00000423798.1:n.277+1193G>A
ENST00000506853.5:n.656+1193G>A
ENST00000510635.1:c.372+86G>A
XM_006714123.2:c.676+86G>A	XP_006714186.1:n.676+86G>A
XR_001741155.2:n.770+86G>A