Canonical Allele Identifier: CA460569204
Gene: THAP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.42698178A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.42843035A>G , CM000670.2:g.42843035A>G GRCh38
NC_000008.10:g.42698178A>G , CM000670.1:g.42698178A>G GRCh37
NC_000008.9:g.42817335A>G NCBI36
NG_011837.1:g.5297T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000254250.7:c.60T>C MANE Select ENSP00000254250.3:p.Val20=
ENST00000345117.2:c.60T>C ENSP00000344966.2:p.Val20=
ENST00000529779.1:c.60T>C ENSP00000433912.1:p.Val20=
NM_018105.2:c.60T>C NP_060575.1:p.Val20=
NM_199003.1:c.60T>C NP_945354.1:p.Val20=
NM_018105.3:c.60T>C MANE Select NP_060575.1:p.Val20=
NM_199003.2:c.60T>C NP_945354.1:p.Val20=
Search 100 bp 5'
Search 100 bp 3'