Canonical Allele Identifier: CA403747849

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8645814A>G (hg19) ; chr19:g.8580930A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8580930A>G , CM000681.2:g.8580930A>G	GRCh38
NC_000019.9:g.8645814A>G , CM000681.1:g.8645814A>G	GRCh37
NC_000019.8:g.8551814A>G	NCBI36
NG_011840.2:g.34773T>C
NG_052844.1:g.1518T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000597188.6:c.3275T>C MANE Select	ENSP00000471851.1:p.Phe1092Ser
ENST00000270328.8:c.3275T>C	ENSP00000270328.4:p.Phe1092Ser
ENST00000593913.5:c.*2152T>C	ENSP00000469901.1:n.*2152T>C
ENST00000595838.5:c.1736T>C	ENSP00000470501.1:p.Phe579Ser
ENST00000597188.5:c.3275T>C	ENSP00000471851.1:p.Phe1092Ser
NM_001282352.1:c.1736T>C	NP_001269281.1:p.Phe579Ser
NM_030957.3:c.3275T>C	NP_112219.3:p.Phe1092Ser
XM_006722917.2:c.2318T>C	XP_006722980.1:p.Phe773Ser
XM_011528331.1:c.3422T>C	XP_011526633.1:p.Phe1141Ser
XM_011528332.1:c.3422T>C	XP_011526634.1:p.Phe1141Ser
XM_011528333.1:c.3422T>C	XP_011526635.1:p.Phe1141Ser
XM_011528334.1:c.3098T>C	XP_011526636.1:p.Phe1033Ser
XM_011528335.1:c.1991T>C	XP_011526637.1:p.Phe664Ser
XM_011528336.1:c.1985T>C	XP_011526638.1:p.Phe662Ser
XM_006722917.3:c.2318T>C	XP_006722980.1:p.Phe773Ser
XM_017027338.2:c.3275T>C	XP_016882827.1:p.Phe1092Ser
XM_017027339.1:c.1844T>C	XP_016882828.1:p.Phe615Ser
XM_017027340.1:c.1838T>C	XP_016882829.1:p.Phe613Ser
NM_030957.4:c.3275T>C MANE Select	NP_112219.3:p.Phe1092Ser
NM_001282352.2:c.1736T>C	NP_001269281.1:p.Phe579Ser