Canonical Allele Identifier: CA403756451

Gene: ADAMTS10

Linked Data

• MyVariant Identifiers: chr19:g.8665823T>A (hg19) ; chr19:g.8600939T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.8600939T>A , CM000681.2:g.8600939T>A	GRCh38
NC_000019.9:g.8665823T>A , CM000681.1:g.8665823T>A	GRCh37
NC_000019.8:g.8571823T>A	NCBI36
NG_011840.2:g.14764A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000597188.6:c.799A>T MANE Select	ENSP00000471851.1:p.Ile267Phe
ENST00000270328.8:c.799A>T	ENSP00000270328.4:p.Ile267Phe
ENST00000593913.5:c.799A>T	ENSP00000469901.1:p.Ile267Phe
ENST00000596466.2:n.748A>T
ENST00000596709.5:n.883A>T
ENST00000596851.5:c.799A>T	ENSP00000469559.1:p.Ile267Phe
ENST00000597188.5:c.799A>T	ENSP00000471851.1:p.Ile267Phe
NM_030957.3:c.799A>T	NP_112219.3:p.Ile267Phe
XM_006722917.2:c.-311A>T	XP_006722980.1:n.-311A>T
XM_011528331.1:c.799A>T	XP_011526633.1:p.Ile267Phe
XM_011528332.1:c.799A>T	XP_011526634.1:p.Ile267Phe
XM_011528333.1:c.799A>T	XP_011526635.1:p.Ile267Phe
XM_011528334.1:c.799A>T	XP_011526636.1:p.Ile267Phe
XR_430156.2:n.1075A>T
XR_936208.1:n.1075A>T
XR_936209.1:n.1075A>T
XM_006722917.3:c.-311A>T	XP_006722980.1:n.-311A>T
XM_017027338.2:c.799A>T	XP_016882827.1:p.Ile267Phe
XR_001753770.1:n.1635A>T
NM_030957.4:c.799A>T MANE Select	NP_112219.3:p.Ile267Phe