Canonical Allele Identifier: CA1768215579
Gene: NAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393630A= , CM000670.2:g.18393630A= GRCh38
NC_000008.10:g.18251140A= , CM000670.1:g.18251140A= GRCh37
NC_000008.9:g.18295420A= NCBI36
NG_012246.1:g.7386A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.-7+2285A= MANE Select ENSP00000286479.3:n.-7+2285A=
ENST00000286479.3:c.-7+2285A= ENSP00000286479.3:n.-7+2285A=
ENST00000520116.1:c.-58+2285A= ENSP00000428416.1:n.-58+2285A=
NM_000015.2:c.-7+2285A= NP_000006.2:n.-7+2285A=
XM_011544358.1:c.-7+894A= XP_011542660.1:n.-7+894A=
XM_017012938.1:c.-6-6368A= XP_016868427.1:n.-6-6368A=
NM_000015.3:c.-7+2285A= MANE Select NP_000006.2:n.-7+2285A=
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