Canonical Allele Identifier: CA1467599901
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313754T= , CM000666.2:g.72313754T= GRCh38
NC_000004.11:g.73179471T= , CM000666.1:g.73179471T= GRCh37
NC_000004.10:g.73398335T= NCBI36
NG_046955.1:g.260046A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286657.10:c.1668A= MANE Select ENSP00000286657.4:p.Ser556=
ENST00000286657.8:c.1668A= ENSP00000286657.4:p.Ser556=
ENST00000622135.1:c.1668A= ENSP00000480055.1:p.Ser556=
NM_014243.2:c.1668A= NP_055058.2:p.Ser556=
XM_011532421.1:c.1611A= XP_011530723.1:p.Ser537=
XM_011532422.1:c.1584A= XP_011530724.1:p.Ser528=
XM_011532423.1:c.1026A= XP_011530725.1:p.Ser342=
XM_011532424.1:c.936A= XP_011530726.1:p.Ser312=
XM_011532421.2:c.1611A= XP_011530723.1:p.Ser537=
XM_011532422.3:c.1584A= XP_011530724.1:p.Ser528=
NM_014243.3:c.1668A= MANE Select NP_055058.2:p.Ser556=