Canonical Allele Identifier: CA1779607941
Gene: THAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1802662699

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42838773C>A , CM000670.2:g.42838773C>A GRCh38
NC_000008.10:g.42693916C>A , CM000670.1:g.42693916C>A GRCh37
NC_000008.9:g.42813073C>A NCBI36
NG_011837.1:g.9559G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.267+413G>T MANE Select ENSP00000254250.3:n.267+413G>T
ENST00000345117.2:c.72-437G>T ENSP00000344966.2:n.72-437G>T
ENST00000529779.1:c.267+413G>T ENSP00000433912.1:n.267+413G>T
NM_018105.2:c.267+413G>T NP_060575.1:n.267+413G>T
NM_199003.1:c.72-437G>T NP_945354.1:n.72-437G>T
NM_018105.3:c.267+413G>T MANE Select NP_060575.1:n.267+413G>T
NM_199003.2:c.72-437G>T NP_945354.1:n.72-437G>T