Canonical Allele Identifier: CA358783033

Gene: AGA

Linked Data

• MyVariant Identifiers: chr4:g.178358674C>G (hg19) ; chr4:g.177437520C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.177437520C>G , CM000666.2:g.177437520C>G	GRCh38
NC_000004.11:g.178358674C>G , CM000666.1:g.178358674C>G	GRCh37
NC_000004.10:g.178595668C>G	NCBI36
NG_011845.2:g.9984G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264595.7:c.508-1G>C MANE Select	ENSP00000264595.2:n.508-1G>C
ENST00000264595.6:c.508-1G>C	ENSP00000264595.2:n.508-1G>C
ENST00000502310.5:c.163-1G>C	ENSP00000423798.1:n.163-1G>C
ENST00000506853.5:n.542-1G>C
ENST00000510635.1:c.204-1G>C
ENST00000510955.5:n.429-1G>C
NM_000027.3:c.508-1G>C	NP_000018.2:n.508-1G>C
NM_001171988.1:c.508-1G>C	NP_001165459.1:n.508-1G>C
NR_033655.1:n.636-1G>C
XM_006714123.2:c.508-1G>C	XP_006714186.1:n.508-1G>C
XR_001741155.2:n.602-1G>C
NM_000027.4:c.508-1G>C MANE Select	NP_000018.2:n.508-1G>C
NM_001171988.2:c.508-1G>C	NP_001165459.1:n.508-1G>C
NR_033655.2:n.570-1G>C