Canonical Allele Identifier: CA403747818

Gene: ADAMTS10

Linked Data

• COSMIC: COSM6420924
• MyVariant Identifiers: chr19:g.8645802C>A (hg19) ; chr19:g.8580918C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580918C>A , CM000681.2:g.8580918C>A	GRCh38
NC_000019.9:g.8645802C>A , CM000681.1:g.8645802C>A	GRCh37
NC_000019.8:g.8551802C>A	NCBI36
NG_011840.2:g.34785G>T
NG_052844.1:g.1530G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3287G>T MANE Select	ENSP00000471851.1:p.Cys1096Phe
ENST00000270328.8:c.3287G>T	ENSP00000270328.4:p.Cys1096Phe
ENST00000593913.5:c.*2164G>T	ENSP00000469901.1:n.*2164G>T
ENST00000595838.5:c.1748G>T	ENSP00000470501.1:p.Cys583Phe
ENST00000597188.5:c.3287G>T	ENSP00000471851.1:p.Cys1096Phe
NM_001282352.1:c.1748G>T	NP_001269281.1:p.Cys583Phe
NM_030957.3:c.3287G>T	NP_112219.3:p.Cys1096Phe
XM_006722917.2:c.2330G>T	XP_006722980.1:p.Cys777Phe
XM_011528331.1:c.3434G>T	XP_011526633.1:p.Cys1145Phe
XM_011528332.1:c.3434G>T	XP_011526634.1:p.Cys1145Phe
XM_011528333.1:c.3434G>T	XP_011526635.1:p.Cys1145Phe
XM_011528334.1:c.3110G>T	XP_011526636.1:p.Cys1037Phe
XM_011528335.1:c.2003G>T	XP_011526637.1:p.Cys668Phe
XM_011528336.1:c.1997G>T	XP_011526638.1:p.Cys666Phe
XM_006722917.3:c.2330G>T	XP_006722980.1:p.Cys777Phe
XM_017027338.2:c.3287G>T	XP_016882827.1:p.Cys1096Phe
XM_017027339.1:c.1856G>T	XP_016882828.1:p.Cys619Phe
XM_017027340.1:c.1850G>T	XP_016882829.1:p.Cys617Phe
NM_030957.4:c.3287G>T MANE Select	NP_112219.3:p.Cys1096Phe
NM_001282352.2:c.1748G>T	NP_001269281.1:p.Cys583Phe