Canonical Allele Identifier: CA2664009566

Gene: AGXT

Linked Data

• gnomAD v4: 2-240875955-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.240875955_240875956insA , CM000664.2:g.240875955_240875956insA	GRCh38
NC_000002.11:g.241815372_241815373insA , CM000664.1:g.241815372_241815373insA	GRCh37
NC_000002.10:g.241464045_241464046insA	NCBI36
NG_008005.1:g.12211_12212insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000307503.4:c.797_798insA MANE Select	ENSP00000302620.3:p.Ile267HisfsTer?
ENST00000307503.3:c.797_798insA	ENSP00000302620.3:p.Ile267HisfsTer?
ENST00000476698.1:n.449_450insA
NM_000030.2:c.797_798insA	NP_000021.1:p.Ile267HisfsTer?
NM_000030.3:c.797_798insA MANE Select	NP_000021.1:p.Ile267HisfsTer?