Canonical Allele Identifier: CA1467599808
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313692T= , CM000666.2:g.72313692T= GRCh38
NC_000004.11:g.73179409T= , CM000666.1:g.73179409T= GRCh37
NC_000004.10:g.73398273T= NCBI36
NG_046955.1:g.260108A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1730A= MANE Select ENSP00000286657.4:p.Gln577=
ENST00000286657.8:c.1730A= ENSP00000286657.4:p.Gln577=
ENST00000622135.1:c.1730A= ENSP00000480055.1:p.Gln577=
NM_014243.2:c.1730A= NP_055058.2:p.Gln577=
XM_011532421.1:c.1673A= XP_011530723.1:p.Gln558=
XM_011532422.1:c.1646A= XP_011530724.1:p.Gln549=
XM_011532423.1:c.1088A= XP_011530725.1:p.Gln363=
XM_011532424.1:c.998A= XP_011530726.1:p.Gln333=
XM_011532421.2:c.1673A= XP_011530723.1:p.Gln558=
XM_011532422.3:c.1646A= XP_011530724.1:p.Gln549=
NM_014243.3:c.1730A= MANE Select NP_055058.2:p.Gln577=