Canonical Allele Identifier: CA1467599745
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313644_72313645delinsCA , CM000666.2:g.72313644_72313645delinsCA GRCh38
NC_000004.11:g.73179361_73179362delinsCA , CM000666.1:g.73179361_73179362delinsCA GRCh37
NC_000004.10:g.73398225_73398226delinsCA NCBI36
NG_046955.1:g.260155_260156delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000286657.10:c.1745+32_1745+33delinsTG MANE Select ENSP00000286657.4:n.1745+32_1745+33delins...
ENST00000286657.8:c.1745+32_1745+33delinsTG ENSP00000286657.4:n.1745+32_1745+33delins...
ENST00000622135.1:c.1745+32_1745+33delinsTG ENSP00000480055.1:n.1745+32_1745+33delins...
NM_014243.2:c.1745+32_1745+33delinsTG NP_055058.2:n.1745+32_1745+33delinsTG
XM_011532421.1:c.1688+32_1688+33delinsTG XP_011530723.1:n.1688+32_1688+33delinsTG
XM_011532422.1:c.1661+32_1661+33delinsTG XP_011530724.1:n.1661+32_1661+33delinsTG
XM_011532423.1:c.1103+32_1103+33delinsTG XP_011530725.1:n.1103+32_1103+33delinsTG
XM_011532424.1:c.1013+32_1013+33delinsTG XP_011530726.1:n.1013+32_1013+33delinsTG
XM_011532421.2:c.1688+32_1688+33delinsTG XP_011530723.1:n.1688+32_1688+33delinsTG
XM_011532422.3:c.1661+32_1661+33delinsTG XP_011530724.1:n.1661+32_1661+33delinsTG
NM_014243.3:c.1745+32_1745+33delinsTG MANE Select NP_055058.2:n.1745+32_1745+33delinsTG