Canonical Allele Identifier: CA2672747100

Gene: AGA

Linked Data

• gnomAD v4: 4-177437313-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437313C>A , CM000666.2:g.177437313C>A	GRCh38
NC_000004.11:g.178358467C>A , CM000666.1:g.178358467C>A	GRCh37
NC_000004.10:g.178595461C>A	NCBI36
NG_011845.2:g.10191G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.622+92G>T MANE Select	ENSP00000264595.2:n.622+92G>T
ENST00000264595.6:c.622+92G>T	ENSP00000264595.2:n.622+92G>T
ENST00000502310.5:c.277+92G>T	ENSP00000423798.1:n.277+92G>T
ENST00000506853.5:n.656+92G>T
ENST00000510635.1:c.318+92G>T
ENST00000510955.5:n.635G>T
NM_000027.3:c.622+92G>T	NP_000018.2:n.622+92G>T
NM_001171988.1:c.622+92G>T	NP_001165459.1:n.622+92G>T
NR_033655.1:n.750+92G>T
XM_006714123.2:c.622+92G>T	XP_006714186.1:n.622+92G>T
XR_001741155.2:n.716+92G>T
NM_000027.4:c.622+92G>T MANE Select	NP_000018.2:n.622+92G>T
NM_001171988.2:c.622+92G>T	NP_001165459.1:n.622+92G>T
NR_033655.2:n.684+92G>T