Canonical Allele Identifier: CA10576134
Community Standard Title: NM_205768.3(ZBTB18):c.1183C>T (p.Gln395Ter)
Gene: ZBTB18 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244054957C>T , CM000663.2:g.244054957C>T GRCh38
NC_000001.10:g.244218259C>T , CM000663.1:g.244218259C>T GRCh37
NC_000001.9:g.242284882C>T NCBI36
NG_033841.1:g.11019C>T

Transcript Alleles

HGVS Amino-acid Change
NM_205768.3:c.1183C>T MANE Select NP_991331.1:p.Gln395Ter
ENST00000358704.4:c.1183C>T MANE Select ENSP00000351539.4:p.Gln395Ter
NM_001278196.1:c.1156C>T NP_001265125.1:p.Gln386Ter
NM_001278196.2:c.1156C>T NP_001265125.1:p.Gln386Ter
NM_006352.4:c.1156C>T NP_006343.2:p.Gln386Ter
NM_205768.2:c.1183C>T NP_991331.1:p.Gln395Ter
ENST00000622512.1:c.1156C>T ENSP00000481278.1:p.Gln386Ter
ENST00000696615.1:c.*360C>T ENSP00000512755.1:n.*360C>T
ENST00000696616.1:c.1156C>T ENSP00000512756.1:p.Gln386Ter
ENST00000696617.1:c.*1113C>T ENSP00000512757.1:n.*1113C>T
ENST00000696618.1:c.1156C>T ENSP00000512758.1:p.Gln386Ter
XM_005273006.2:c.1156C>T XP_005273063.1:p.Gln386Ter
XM_017000060.1:c.1156C>T XP_016855549.1:p.Gln386Ter