Canonical Allele Identifier: CA1779607952

Gene: THAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.42838789G= , CM000670.2:g.42838789G=	GRCh38
NC_000008.10:g.42693932G= , CM000670.1:g.42693932G=	GRCh37
NC_000008.9:g.42813089G=	NCBI36
NG_011837.1:g.9543C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254250.7:c.267+397C= MANE Select	ENSP00000254250.3:n.267+397C=
ENST00000345117.2:c.72-453C=	ENSP00000344966.2:n.72-453C=
ENST00000529779.1:c.267+397C=	ENSP00000433912.1:n.267+397C=
NM_018105.2:c.267+397C=	NP_060575.1:n.267+397C=
NM_199003.1:c.72-453C=	NP_945354.1:n.72-453C=
NM_018105.3:c.267+397C= MANE Select	NP_060575.1:n.267+397C=
NM_199003.2:c.72-453C=	NP_945354.1:n.72-453C=