Canonical Allele Identifier: CA13548174

Gene: SCUBE2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.9090011A>G , CM000673.2:g.9090011A>G	GRCh38
NC_000011.9:g.9111558A>G , CM000673.1:g.9111558A>G	GRCh37
NC_000011.8:g.9068134A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649792.2:c.134-182T>C MANE Select	ENSP00000497523.1:n.134-182T>C
ENST00000309263.7:c.134-182T>C	ENSP00000310658.3:n.134-182T>C
ENST00000450649.6:c.134-182T>C	ENSP00000415187.2:n.134-182T>C
ENST00000520467.5:c.134-182T>C	ENSP00000429969.1:n.134-182T>C
ENST00000534295.1:n.408-182T>C
NM_001170690.1:c.134-182T>C	NP_001164161.1:n.134-182T>C
NM_020974.2:c.134-182T>C	NP_066025.2:n.134-182T>C
XM_005253032.3:c.134-182T>C	XP_005253089.2:n.134-182T>C
XM_005253033.3:c.134-182T>C	XP_005253090.2:n.134-182T>C
XM_005253034.3:c.134-182T>C	XP_005253091.2:n.134-182T>C
XM_005253035.3:c.134-182T>C	XP_005253092.2:n.134-182T>C
XM_005253036.3:c.134-182T>C	XP_005253093.2:n.134-182T>C
XM_005253037.3:c.134-182T>C	XP_005253094.2:n.134-182T>C
XM_006718268.2:c.134-182T>C	XP_006718331.1:n.134-182T>C
XM_011520246.1:c.134-182T>C	XP_011518548.1:n.134-182T>C
XM_011520247.1:c.134-182T>C	XP_011518549.1:n.134-182T>C
XM_011520248.1:c.134-182T>C	XP_011518550.1:n.134-182T>C
NM_001330199.1:c.134-182T>C	NP_001317128.1:n.134-182T>C
XM_005253032.4:c.134-182T>C	XP_005253089.2:n.134-182T>C
XM_005253034.4:c.134-182T>C	XP_005253091.2:n.134-182T>C
XM_005253035.4:c.134-182T>C	XP_005253092.2:n.134-182T>C
XM_005253036.4:c.134-182T>C	XP_005253093.2:n.134-182T>C
XM_005253037.4:c.134-182T>C	XP_005253094.2:n.134-182T>C
XM_011520246.2:c.134-182T>C	XP_011518548.1:n.134-182T>C
XM_011520247.2:c.134-182T>C	XP_011518549.1:n.134-182T>C
XM_011520248.2:c.134-182T>C	XP_011518550.1:n.134-182T>C
XM_017018080.1:c.134-182T>C	XP_016873569.1:n.134-182T>C
XM_017018081.1:c.134-182T>C	XP_016873570.1:n.134-182T>C
XM_017018082.2:c.134-182T>C	XP_016873571.1:n.134-182T>C
NM_001367977.1:c.134-182T>C	NP_001354906.1:n.134-182T>C
NM_001170690.2:c.134-182T>C	NP_001164161.1:n.134-182T>C
NM_001330199.2:c.134-182T>C	NP_001317128.1:n.134-182T>C
NM_001367977.2:c.134-182T>C MANE Select	NP_001354906.1:n.134-182T>C
NM_020974.3:c.134-182T>C	NP_066025.2:n.134-182T>C
NM_001170690.3:c.134-182T>C	NP_001164161.1:n.134-182T>C
NM_001330199.3:c.134-182T>C	NP_001317128.1:n.134-182T>C
NM_020974.4:c.134-182T>C	NP_066025.2:n.134-182T>C