Canonical Allele Identifier: CA15848988

Gene: THSD4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71316280A>C , CM000677.2:g.71316280A>C	GRCh38
NC_000015.9:g.71608619A>C , CM000677.1:g.71608619A>C	GRCh37
NC_000015.8:g.69395673A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261862.8:c.1015+59565A>C MANE Select	ENSP00000261862.8:n.1015+59565A>C
ENST00000355327.7:c.1015+59565A>C	ENSP00000347484.3:n.1015+59565A>C
NM_024817.2:c.1015+59565A>C	NP_079093.2:n.1015+59565A>C
XM_006720692.2:c.1015+59565A>C	XP_006720755.1:n.1015+59565A>C
XM_006720692.3:c.1015+59565A>C	XP_006720755.1:n.1015+59565A>C
XM_017022582.2:c.270+59565A>C	XP_016878071.1:n.270+59565A>C
XM_017022583.1:c.37+59565A>C	XP_016878072.1:n.37+59565A>C
XM_017022585.1:c.120+59565A>C	XP_016878074.1:n.120+59565A>C
NM_001394532.1:c.1015+59565A>C	NP_001381461.1:n.1015+59565A>C
NM_024817.3:c.1015+59565A>C MANE Select	NP_079093.2:n.1015+59565A>C