Canonical Allele Identifier: CA1768215619
Gene: NAT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393720T= , CM000670.2:g.18393720T= GRCh38
NC_000008.10:g.18251230T= , CM000670.1:g.18251230T= GRCh37
NC_000008.9:g.18295510T= NCBI36
NG_012246.1:g.7476T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286479.4:c.-7+2375T= MANE Select ENSP00000286479.3:n.-7+2375T=
ENST00000286479.3:c.-7+2375T= ENSP00000286479.3:n.-7+2375T=
ENST00000520116.1:c.-58+2375T= ENSP00000428416.1:n.-58+2375T=
NM_000015.2:c.-7+2375T= NP_000006.2:n.-7+2375T=
XM_011544358.1:c.-7+984T= XP_011542660.1:n.-7+984T=
XM_017012938.1:c.-6-6278T= XP_016868427.1:n.-6-6278T=
NM_000015.3:c.-7+2375T= MANE Select NP_000006.2:n.-7+2375T=
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