Canonical Allele Identifier: CA1768215389
Gene: NAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393238A= , CM000670.2:g.18393238A= GRCh38
NC_000008.10:g.18250748A= , CM000670.1:g.18250748A= GRCh37
NC_000008.9:g.18295028A= NCBI36
NG_012246.1:g.6994A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.-7+1893A= MANE Select ENSP00000286479.3:n.-7+1893A=
ENST00000286479.3:c.-7+1893A= ENSP00000286479.3:n.-7+1893A=
ENST00000520116.1:c.-58+1893A= ENSP00000428416.1:n.-58+1893A=
NM_000015.2:c.-7+1893A= NP_000006.2:n.-7+1893A=
XM_011544358.1:c.-7+502A= XP_011542660.1:n.-7+502A=
XM_017012938.1:c.-7+6202A= XP_016868427.1:n.-7+6202A=
NM_000015.3:c.-7+1893A= MANE Select NP_000006.2:n.-7+1893A=
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