Canonical Allele Identifier: CA129664
Community Standard Title: NM_014797.3(ZBTB24):c.1222T>G (p.Cys408Gly)
Gene: ZBTB24 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.109475465A>C , CM000668.2:g.109475465A>C GRCh38
NC_000006.11:g.109796668A>C , CM000668.1:g.109796668A>C GRCh37
NC_000006.10:g.109903361A>C NCBI36
NG_029388.1:g.12773T>G , LRG_326:g.12773T>G

Transcript Alleles

HGVS Amino-acid Change
NM_014797.3:c.1222T>G MANE Select NP_055612.2:p.Cys408Gly
ENST00000230122.4:c.1222T>G MANE Select ENSP00000230122.4:p.Cys408Gly
NM_014797.2:c.1222T>G , LRG_326t1:c.1222T>G NP_055612.2:p.Cys408Gly
ENST00000230122.3:c.1222T>G ENSP00000230122.3:p.Cys408Gly
ENST00000698513.1:c.1054T>G ENSP00000513763.1:p.Cys352Gly
ENST00000698514.1:c.*80T>G ENSP00000513764.1:n.*80T>G
ENST00000698515.1:c.*80T>G ENSP00000513765.1:n.*80T>G
ENST00000698516.1:c.1222T>G ENSP00000513766.1:p.Cys408Gly
ENST00000698517.1:n.2062T>G
ENST00000698518.1:c.1222T>G ENSP00000513767.1:p.Cys408Gly
ENST00000698519.1:c.1054T>G ENSP00000513768.1:p.Cys352Gly
ENST00000698520.1:c.952+5610T>G ENSP00000513769.1:n.952+5610T>G