Canonical Allele Identifier: CA2701624370
Gene: AGXT HGNC NCBI

Linked Data

dbSNP Id: rs180177209

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240869418_240869426dup , CM000664.2:g.240869418_240869426dup GRCh38
NC_000002.11:g.241808835_241808843dup , CM000664.1:g.241808835_241808843dup GRCh37
NC_000002.10:g.241457508_241457516dup NCBI36
NG_008005.1:g.5674_5682dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.358+56_358+64dup MANE Select ENSP00000302620.3:n.358+56_358+64dup
ENST00000307503.3:c.358+56_358+64dup ENSP00000302620.3:n.358+56_358+64dup
ENST00000472436.1:n.378+56_378+64dup
NM_000030.2:c.358+56_358+64dup NP_000021.1:n.358+56_358+64dup
XR_924060.1:n.405+816_405+824dup
NM_000030.3:c.358+56_358+64dup MANE Select NP_000021.1:n.358+56_358+64dup