Canonical Allele Identifier: CA371107660
Gene: THAP1 HGNC NCBI

Linked Data

gnomAD v4: 8-42839189-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42839189G>C , CM000670.2:g.42839189G>C GRCh38
NC_000008.10:g.42694332G>C , CM000670.1:g.42694332G>C GRCh37
NC_000008.9:g.42813489G>C NCBI36
NG_011837.1:g.9143C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.264C>G MANE Select ENSP00000254250.3:p.Asp88Glu
ENST00000345117.2:c.72-853C>G ENSP00000344966.2:n.72-853C>G
ENST00000529779.1:c.264C>G ENSP00000433912.1:p.Asp88Glu
NM_018105.2:c.264C>G NP_060575.1:p.Asp88Glu
NM_199003.1:c.72-853C>G NP_945354.1:n.72-853C>G
NM_018105.3:c.264C>G MANE Select NP_060575.1:p.Asp88Glu
NM_199003.2:c.72-853C>G NP_945354.1:n.72-853C>G