Canonical Allele Identifier: CA645538648

Gene: AGXT

Linked Data

• COSMIC: COSM5917513

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240869035G>A , CM000664.2:g.240869035G>A	GRCh38
NC_000002.11:g.241808452G>A , CM000664.1:g.241808452G>A	GRCh37
NC_000002.10:g.241457125G>A	NCBI36
NG_008005.1:g.5291G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000307503.4:c.165+5G>A MANE Select	ENSP00000302620.3:n.165+5G>A
ENST00000307503.3:c.165+5G>A	ENSP00000302620.3:n.165+5G>A
ENST00000472436.1:n.185+5G>A
NM_000030.2:c.165+5G>A	NP_000021.1:n.165+5G>A
XR_924060.1:n.405+1198C>T
NM_000030.3:c.165+5G>A MANE Select	NP_000021.1:n.165+5G>A