Canonical Allele Identifier: CA1768218851

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400192_18400194delinsCCG , CM000670.2:g.18400192_18400194delinsCCG	GRCh38
NC_000008.10:g.18257702_18257704delinsCCG , CM000670.1:g.18257702_18257704delinsCCG	GRCh37
NC_000008.9:g.18301982_18301984delinsCCG	NCBI36
NG_012246.1:g.13948_13950delinsCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.189_191delinsCCG MANE Select	ENSP00000286479.3:p.Asn63=
ENST00000286479.3:c.189_191delinsCCG	ENSP00000286479.3:p.Asn63=
ENST00000520116.1:c.-57-145_-57-143delinsCCG	ENSP00000428416.1:n.-57-145_-57-143delinsCCG
NM_000015.2:c.189_191delinsCCG	NP_000006.2:p.Asn63=
XM_011544358.1:c.189_191delinsCCG	XP_011542660.1:p.Asn63=
XM_017012938.1:c.189_191delinsCCG	XP_016868427.1:p.Asn63=
NM_000015.3:c.189_191delinsCCG MANE Select	NP_000006.2:p.Asn63=