Canonical Allele Identifier: CA2520812208
Gene: NAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.18393324A>T , CM000670.2:g.18393324A>T GRCh38
NC_000008.10:g.18250834A>T , CM000670.1:g.18250834A>T GRCh37
NC_000008.9:g.18295114A>T NCBI36
NG_012246.1:g.7080A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286479.4:c.-7+1979A>T MANE Select ENSP00000286479.3:n.-7+1979A>T
ENST00000286479.3:c.-7+1979A>T ENSP00000286479.3:n.-7+1979A>T
ENST00000520116.1:c.-58+1979A>T ENSP00000428416.1:n.-58+1979A>T
NM_000015.2:c.-7+1979A>T NP_000006.2:n.-7+1979A>T
XM_011544358.1:c.-7+588A>T XP_011542660.1:n.-7+588A>T
XM_017012938.1:c.-7+6288A>T XP_016868427.1:n.-7+6288A>T
NM_000015.3:c.-7+1979A>T MANE Select NP_000006.2:n.-7+1979A>T