Canonical Allele Identifier: CA305002572

Gene: ADAMTS10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8605046C>G , CM000681.2:g.8605046C>G	GRCh38
NG_011840.2:g.10657G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.401G>C MANE Select	ENSP00000471851.1:p.Ser134Thr
ENST00000270328.8:c.401G>C	ENSP00000270328.4:p.Ser134Thr
ENST00000593534.1:n.520G>C
ENST00000593913.5:c.401G>C	ENSP00000469901.1:p.Ser134Thr
ENST00000596466.2:n.350G>C
ENST00000596709.5:n.485G>C
ENST00000596851.5:c.401G>C	ENSP00000469559.1:p.Ser134Thr
ENST00000597188.5:c.401G>C	ENSP00000471851.1:p.Ser134Thr
NM_030957.3:c.401G>C	NP_112219.3:p.Ser134Thr
XM_006722917.2:c.-709G>C	XP_006722980.1:n.-709G>C
XM_011528331.1:c.401G>C	XP_011526633.1:p.Ser134Thr
XM_011528332.1:c.401G>C	XP_011526634.1:p.Ser134Thr
XM_011528333.1:c.401G>C	XP_011526635.1:p.Ser134Thr
XM_011528334.1:c.401G>C	XP_011526636.1:p.Ser134Thr
XR_430156.2:n.677G>C
XR_936208.1:n.677G>C
XR_936209.1:n.677G>C
XM_006722917.3:c.-709G>C	XP_006722980.1:n.-709G>C
XM_017027338.2:c.401G>C	XP_016882827.1:p.Ser134Thr
XR_001753770.1:n.1237G>C
NM_030957.4:c.401G>C MANE Select	NP_112219.3:p.Ser134Thr