Canonical Allele Identifier: CA1768215393

Gene: NAT2

Linked Data

• dbSNP Id: rs1800619522

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.18393243_18393246del , CM000670.2:g.18393243_18393246del	GRCh38
NC_000008.10:g.18250753_18250756del , CM000670.1:g.18250753_18250756del	GRCh37
NC_000008.9:g.18295033_18295036del	NCBI36
NG_012246.1:g.6999_7002del

Transcript Alleles

HGVS	Amino-acid change
ENST00000286479.4:c.-7+1898_-7+1901del MANE Select	ENSP00000286479.3:n.-7+1898_-7+1901del
ENST00000286479.3:c.-7+1898_-7+1901del	ENSP00000286479.3:n.-7+1898_-7+1901del
ENST00000520116.1:c.-58+1898_-58+1901del	ENSP00000428416.1:n.-58+1898_-58+1901del
NM_000015.2:c.-7+1898_-7+1901del	NP_000006.2:n.-7+1898_-7+1901del
XM_011544358.1:c.-7+507_-7+510del	XP_011542660.1:n.-7+507_-7+510del
XM_017012938.1:c.-7+6207_-7+6210del	XP_016868427.1:n.-7+6207_-7+6210del
NM_000015.3:c.-7+1898_-7+1901del MANE Select	NP_000006.2:n.-7+1898_-7+1901del