Canonical Allele Identifier: CA2838231915

Gene: THSD4

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.71467644G>T , CM000677.2:g.71467644G>T	GRCh38
NC_000015.9:g.71759983G>T , CM000677.1:g.71759983G>T	GRCh37
NC_000015.8:g.69547037G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261862.8:c.1152+55821G>T MANE Select	ENSP00000261862.8:n.1152+55821G>T
ENST00000355327.7:c.1152+55821G>T	ENSP00000347484.3:n.1152+55821G>T
NM_024817.2:c.1152+55821G>T	NP_079093.2:n.1152+55821G>T
XM_006720692.2:c.1152+55821G>T	XP_006720755.1:n.1152+55821G>T
XM_011522044.1:c.144+55821G>T	XP_011520346.1:n.144+55821G>T
XM_006720692.3:c.1152+55821G>T	XP_006720755.1:n.1152+55821G>T
XM_011522044.2:c.144+55821G>T	XP_011520346.1:n.144+55821G>T
XM_017022582.2:c.271-192886G>T	XP_016878071.1:n.271-192886G>T
XM_017022583.1:c.174+55821G>T	XP_016878072.1:n.174+55821G>T
XM_017022585.1:c.121-192886G>T	XP_016878074.1:n.121-192886G>T
XM_017022586.1:c.99+55821G>T	XP_016878075.1:n.99+55821G>T
NM_001394532.1:c.1152+55821G>T	NP_001381461.1:n.1152+55821G>T
NM_024817.3:c.1152+55821G>T MANE Select	NP_079093.2:n.1152+55821G>T