Canonical Allele Identifier: CA357430832
Gene: ADAMTS3 HGNC NCBI

Linked Data

dbSNP Id: rs1719309874

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313743A>G , CM000666.2:g.72313743A>G GRCh38
NC_000004.11:g.73179460A>G , CM000666.1:g.73179460A>G GRCh37
NC_000004.10:g.73398324A>G NCBI36
NG_046955.1:g.260057T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1679T>C MANE Select ENSP00000286657.4:p.Phe560Ser
ENST00000286657.8:c.1679T>C ENSP00000286657.4:p.Phe560Ser
ENST00000622135.1:c.1679T>C ENSP00000480055.1:p.Phe560Ser
NM_014243.2:c.1679T>C NP_055058.2:p.Phe560Ser
XM_011532421.1:c.1622T>C XP_011530723.1:p.Phe541Ser
XM_011532422.1:c.1595T>C XP_011530724.1:p.Phe532Ser
XM_011532423.1:c.1037T>C XP_011530725.1:p.Phe346Ser
XM_011532424.1:c.947T>C XP_011530726.1:p.Phe316Ser
XM_011532421.2:c.1622T>C XP_011530723.1:p.Phe541Ser
XM_011532422.3:c.1595T>C XP_011530724.1:p.Phe532Ser
NM_014243.3:c.1679T>C MANE Select NP_055058.2:p.Phe560Ser