Canonical Allele Identifier: CA2701850887

Gene: AGXT

Linked Data

• dbSNP Id: rs2106427723

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240869408_240869416del , CM000664.2:g.240869408_240869416del	GRCh38
NC_000002.11:g.241808825_241808833del , CM000664.1:g.241808825_241808833del	GRCh37
NC_000002.10:g.241457498_241457506del	NCBI36
NG_008005.1:g.5664_5672del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.358+46_358+54del MANE Select	ENSP00000302620.3:n.358+46_358+54del
ENST00000307503.3:c.358+46_358+54del	ENSP00000302620.3:n.358+46_358+54del
ENST00000472436.1:n.378+46_378+54del
NM_000030.2:c.358+46_358+54del	NP_000021.1:n.358+46_358+54del
XR_924060.1:n.405+817_405+825del
NM_000030.3:c.358+46_358+54del MANE Select	NP_000021.1:n.358+46_358+54del