Canonical Allele Identifier: CA2532063647

Gene: NAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18393396_18393397insCT , CM000670.2:g.18393396_18393397insCT	GRCh38
NC_000008.10:g.18250906_18250907insCT , CM000670.1:g.18250906_18250907insCT	GRCh37
NC_000008.9:g.18295186_18295187insCT	NCBI36
NG_012246.1:g.7152_7153insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286479.4:c.-7+2051_-7+2052insCT MANE Select	ENSP00000286479.3:n.-7+2051_-7+2052insCT
ENST00000286479.3:c.-7+2051_-7+2052insCT	ENSP00000286479.3:n.-7+2051_-7+2052insCT
ENST00000520116.1:c.-58+2051_-58+2052insCT	ENSP00000428416.1:n.-58+2051_-58+2052insCT
NM_000015.2:c.-7+2051_-7+2052insCT	NP_000006.2:n.-7+2051_-7+2052insCT
XM_011544358.1:c.-7+660_-7+661insCT	XP_011542660.1:n.-7+660_-7+661insCT
XM_017012938.1:c.-7+6360_-7+6361insCT	XP_016868427.1:n.-7+6360_-7+6361insCT
NM_000015.3:c.-7+2051_-7+2052insCT MANE Select	NP_000006.2:n.-7+2051_-7+2052insCT