Canonical Allele Identifier: CA2199786994
Gene: ADAMTS17 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.99973028T= , CM000677.2:g.99973028T= GRCh38
NC_000015.9:g.100513233T= , CM000677.1:g.100513233T= GRCh37
NC_000015.8:g.98330756T= NCBI36
NG_016287.1:g.373951A=
NG_016287.2:g.373951A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000268070.9:c.*1374A= MANE Select ENSP00000268070.4:n.*1374A=
ENST00000268070.8:c.*1374A= ENSP00000268070.4:n.*1374A=
ENST00000557896.1:n.1673A=
NM_139057.2:c.*1374A= NP_620688.2:n.*1374A=
XM_005254872.2:c.*1374A= XP_005254929.1:n.*1374A=
XM_011521312.1:c.*1374A= XP_011519614.1:n.*1374A=
XR_429624.2:n.1743+295T=
NM_139057.3:c.*1374A= NP_620688.2:n.*1374A=
XM_005254872.3:c.*1374A= XP_005254929.1:n.*1374A=
XM_011521312.2:c.*1374A= XP_011519614.1:n.*1374A=
XM_017021973.2:c.*1374A= XP_016877462.1:n.*1374A=
XM_017021975.1:c.*1374A= XP_016877464.1:n.*1374A=
XM_017021976.1:c.*1374A= XP_016877465.1:n.*1374A=
XM_017021978.1:c.*1374A= XP_016877467.1:n.*1374A=
XM_017021979.1:c.*1374A= XP_016877468.1:n.*1374A=
XM_017021980.1:c.*1374A= XP_016877469.1:n.*1374A=
XM_017021982.1:c.*1374A= XP_016877471.1:n.*1374A=
XM_017021983.1:c.*1374A= XP_016877472.1:n.*1374A=
NM_139057.4:c.*1374A= MANE Select NP_620688.2:n.*1374A=