Canonical Allele Identifier: CA403756076

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8661961C>G (hg19) ; chr19:g.8597077C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8597077C>G , CM000681.2:g.8597077C>G	GRCh38
NC_000019.9:g.8661961C>G , CM000681.1:g.8661961C>G	GRCh37
NC_000019.8:g.8567961C>G	NCBI36
NG_011840.2:g.18626G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.950G>C MANE Select	ENSP00000471851.1:p.Trp317Ser
ENST00000270328.8:c.950G>C	ENSP00000270328.4:p.Trp317Ser
ENST00000593913.5:c.*78+7G>C	ENSP00000469901.1:n.*78+7G>C
ENST00000596851.5:c.*85G>C	ENSP00000469559.1:n.*85G>C
ENST00000597188.5:c.950G>C	ENSP00000471851.1:p.Trp317Ser
ENST00000601163.1:n.145G>C
NM_030957.3:c.950G>C	NP_112219.3:p.Trp317Ser
XM_006722917.2:c.-155G>C	XP_006722980.1:n.-155G>C
XM_011528331.1:c.950G>C	XP_011526633.1:p.Trp317Ser
XM_011528332.1:c.950G>C	XP_011526634.1:p.Trp317Ser
XM_011528333.1:c.950G>C	XP_011526635.1:p.Trp317Ser
XM_011528334.1:c.950G>C	XP_011526636.1:p.Trp317Ser
XR_430156.2:n.1226G>C
XR_936208.1:n.1226G>C
XR_936209.1:n.1226G>C
XM_006722917.3:c.-155G>C	XP_006722980.1:n.-155G>C
XM_017027338.2:c.950G>C	XP_016882827.1:p.Trp317Ser
XR_001753770.1:n.1786G>C
NM_030957.4:c.950G>C MANE Select	NP_112219.3:p.Trp317Ser