Canonical Allele Identifier: CA589201377

Gene: SUSD3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.93082870C>G , CM000671.2:g.93082870C>G	GRCh38
NC_000009.11:g.95845152C>G , CM000671.1:g.95845152C>G	GRCh37
NC_000009.10:g.94884973C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375472.8:c.558-1667C>G MANE Select	ENSP00000364621.3:n.558-1667C>G
ENST00000375469.5:c.519-1667C>G	ENSP00000364618.1:n.519-1667C>G
ENST00000375472.7:c.558-1667C>G	ENSP00000364621.3:n.558-1667C>G
ENST00000465709.5:c.333-1667C>G	ENSP00000475051.1:n.333-1667C>G
ENST00000471462.2:c.149-1667C>G
ENST00000617293.4:c.426-1667C>G	ENSP00000479555.1:n.426-1667C>G
NM_001287005.1:c.519-1667C>G	NP_001273934.1:n.519-1667C>G
NM_001287006.1:c.426-1667C>G	NP_001273935.1:n.426-1667C>G
NM_001287007.1:c.237-1667C>G	NP_001273936.1:n.237-1667C>G
NM_001287008.1:c.369-1667C>G	NP_001273937.1:n.369-1667C>G
NM_145006.3:c.558-1667C>G	NP_659443.1:n.558-1667C>G
XM_011518358.1:c.519-1667C>G	XP_011516660.1:n.519-1667C>G
XM_011518359.1:c.519-1667C>G	XP_011516661.1:n.519-1667C>G
XM_011518360.1:c.519-1667C>G	XP_011516662.1:n.519-1667C>G
XM_011518361.1:c.519-1667C>G	XP_011516663.1:n.519-1667C>G
XM_011518362.1:c.387-1667C>G	XP_011516664.1:n.387-1667C>G
XM_011518361.2:c.519-1667C>G	XP_011516663.1:n.519-1667C>G
XM_017014448.1:c.606-1667C>G	XP_016869937.1:n.606-1667C>G
XM_017014449.1:c.606-1667C>G	XP_016869938.1:n.606-1667C>G
XM_017014450.1:c.519-1667C>G	XP_016869939.1:n.519-1667C>G
XM_017014451.2:c.492-1667C>G	XP_016869940.1:n.492-1667C>G
NM_145006.4:c.558-1667C>G MANE Select	NP_659443.1:n.558-1667C>G
NM_001287005.2:c.519-1667C>G	NP_001273934.1:n.519-1667C>G
NM_001287007.2:c.237-1667C>G	NP_001273936.1:n.237-1667C>G
NM_001287008.2:c.369-1667C>G	NP_001273937.1:n.369-1667C>G
NM_001287006.2:c.426-1667C>G	NP_001273935.1:n.426-1667C>G