Canonical Allele Identifier: CA1768215478
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393415G= , CM000670.2:g.18393415G= GRCh38
NC_000008.10:g.18250925G= , CM000670.1:g.18250925G= GRCh37
NC_000008.9:g.18295205G= NCBI36
NG_012246.1:g.7171G=

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+2070G= MANE Select ENSP00000286479.3:n.-7+2070G=
ENST00000286479.3:c.-7+2070G= ENSP00000286479.3:n.-7+2070G=
ENST00000520116.1:c.-58+2070G= ENSP00000428416.1:n.-58+2070G=
NM_000015.2:c.-7+2070G= NP_000006.2:n.-7+2070G=
XM_011544358.1:c.-7+679G= XP_011542660.1:n.-7+679G=
XM_017012938.1:c.-7+6379G= XP_016868427.1:n.-7+6379G=
NM_000015.3:c.-7+2070G= MANE Select NP_000006.2:n.-7+2070G=