Canonical Allele Identifier: CA1768215492
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393442G= , CM000670.2:g.18393442G= GRCh38
NC_000008.10:g.18250952G= , CM000670.1:g.18250952G= GRCh37
NC_000008.9:g.18295232G= NCBI36
NG_012246.1:g.7198G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+2097G= MANE Select ENSP00000286479.3:n.-7+2097G=
ENST00000286479.3:c.-7+2097G= ENSP00000286479.3:n.-7+2097G=
ENST00000520116.1:c.-58+2097G= ENSP00000428416.1:n.-58+2097G=
NM_000015.2:c.-7+2097G= NP_000006.2:n.-7+2097G=
XM_011544358.1:c.-7+706G= XP_011542660.1:n.-7+706G=
XM_017012938.1:c.-7+6406G= XP_016868427.1:n.-7+6406G=
NM_000015.3:c.-7+2097G= MANE Select NP_000006.2:n.-7+2097G=