Canonical Allele Identifier: CA647781034
Gene: AGXT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.240868837_240868838insA , CM000664.2:g.240868837_240868838insA GRCh38
NC_000002.11:g.241808254_241808255insA , CM000664.1:g.241808254_241808255insA GRCh37
NC_000002.10:g.241456927_241456928insA NCBI36
NG_008005.1:g.5093_5094insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307503.4:c.-29_-28insA MANE Select ENSP00000302620.3:n.-29_-28insA
ENST00000307503.3:c.-29_-28insA ENSP00000302620.3:n.-29_-28insA
NM_000030.2:c.-29_-28insA NP_000021.1:n.-29_-28insA
XR_924060.1:n.405+1395_405+1396insT
NM_000030.3:c.-29_-28insA MANE Select NP_000021.1:n.-29_-28insA