Canonical Allele Identifier: CA2838464133

Gene: THAP4

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.241602013G>T , CM000664.2:g.241602013G>T	GRCh38
NC_000002.11:g.242541428G>T , CM000664.1:g.242541428G>T	GRCh37
NC_000002.10:g.242190101G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000407315.6:c.1511-14C>A MANE Select	ENSP00000385006.1:n.1511-14C>A
ENST00000321679.4:n.158C>A
ENST00000402136.5:c.275-14C>A	ENSP00000385931.1:n.275-14C>A
ENST00000402545.5:c.275-14C>A	ENSP00000384352.1:n.275-14C>A
ENST00000407315.5:c.1511-14C>A	ENSP00000385006.1:n.1511-14C>A
ENST00000497486.1:n.26-14C>A
ENST00000612200.1:c.496+996C>A	ENSP00000482312.1:n.496+996C>A
NM_001164356.1:c.275-14C>A	NP_001157828.1:n.275-14C>A
NM_015963.5:c.1511-14C>A	NP_057047.4:n.1511-14C>A
XM_005247016.3:c.1511-14C>A	XP_005247073.2:n.1511-14C>A
XM_011511291.1:c.1583-14C>A	XP_011509593.1:n.1583-14C>A
XM_005247016.4:c.1832-14C>A	XP_005247073.3:n.1832-14C>A
XM_011511291.2:c.1583-14C>A	XP_011509593.1:n.1583-14C>A
XM_017004256.1:c.1583-14C>A	XP_016859745.1:n.1583-14C>A
NM_015963.6:c.1511-14C>A MANE Select	NP_057047.4:n.1511-14C>A
NM_001164356.2:c.275-14C>A	NP_001157828.1:n.275-14C>A