Canonical Allele Identifier: CA15530702

Gene: THSD7A

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.11524758C>G , CM000669.2:g.11524758C>G	GRCh38
NC_000007.13:g.11564385C>G , CM000669.1:g.11564385C>G	GRCh37
NC_000007.12:g.11530910C>G	NCBI36
NG_027670.1:g.312440G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423059.9:c.1822+16661G>C MANE Select	ENSP00000406482.2:n.1822+16661G>C
ENST00000423059.8:c.1822+16661G>C	ENSP00000406482.2:n.1822+16661G>C
ENST00000497575.1:n.311+16661G>C
ENST00000617773.1:c.1822+16661G>C	ENSP00000481440.1:n.1822+16661G>C
NM_015204.2:c.1822+16661G>C	NP_056019.1:n.1822+16661G>C
XM_006715659.1:c.1822+16661G>C	XP_006715722.1:n.1822+16661G>C
XM_006715660.1:c.1822+16661G>C	XP_006715723.1:n.1822+16661G>C
XM_006715661.2:c.1822+16661G>C	XP_006715724.1:n.1822+16661G>C
XM_006715662.1:c.1822+16661G>C	XP_006715725.1:n.1822+16661G>C
XM_011515193.1:c.1615+16661G>C	XP_011513495.1:n.1615+16661G>C
XM_011515194.1:c.1615+16661G>C	XP_011513496.1:n.1615+16661G>C
XM_011515195.1:c.1822+16661G>C	XP_011513497.1:n.1822+16661G>C
XM_011515193.3:c.1615+16661G>C	XP_011513495.1:n.1615+16661G>C
XR_001744589.1:n.2073+16661G>C
NM_015204.3:c.1822+16661G>C MANE Select	NP_056019.1:n.1822+16661G>C