Canonical Allele Identifier: CA1768218929

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18400327_18400330delinsTCTC , CM000670.2:g.18400327_18400330delinsTCTC	GRCh38
NC_000008.10:g.18257837_18257840delinsTCTC , CM000670.1:g.18257837_18257840delinsTCTC	GRCh37
NC_000008.9:g.18302117_18302120delinsTCTC	NCBI36
NG_012246.1:g.14083_14086delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.324_327delinsTCTC MANE Select	ENSP00000286479.3:p.Leu108=
ENST00000286479.3:c.324_327delinsTCTC	ENSP00000286479.3:p.Leu108=
ENST00000520116.1:c.-57-10_-57-7delinsTCTC	ENSP00000428416.1:n.-57-10_-57-7delinsTCTC
NM_000015.2:c.324_327delinsTCTC	NP_000006.2:p.Leu108=
XM_011544358.1:c.324_327delinsTCTC	XP_011542660.1:p.Leu108=
XM_017012938.1:c.324_327delinsTCTC	XP_016868427.1:p.Leu108=
NM_000015.3:c.324_327delinsTCTC MANE Select	NP_000006.2:p.Leu108=