Canonical Allele Identifier: CA5540309
Gene: ADAMTS14 HGNC NCBI

Linked Data

dbSNP Id: rs764824205

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.70758038G>A , CM000672.2:g.70758038G>A GRCh38
NC_000010.10:g.72517794G>A , CM000672.1:g.72517794G>A GRCh37
NC_000010.9:g.72187800G>A NCBI36
NG_042147.1:g.90236G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000373207.2:c.3014G>A MANE Select ENSP00000362303.1:p.Cys1005Tyr
ENST00000373207.1:c.3014G>A ENSP00000362303.1:p.Cys1005Tyr
ENST00000373208.5:c.3023G>A ENSP00000362304.1:p.Cys1008Tyr
NM_080722.3:c.3014G>A NP_542453.2:p.Cys1005Tyr
NM_139155.2:c.3023G>A NP_631894.2:p.Cys1008Tyr
XM_011539300.1:c.2513G>A XP_011537602.1:p.Cys838Tyr
XM_011539301.1:c.2087G>A XP_011537603.1:p.Cys696Tyr
XM_011539302.1:c.2087G>A XP_011537604.1:p.Cys696Tyr
XM_011539309.1:c.1583G>A XP_011537611.1:p.Cys528Tyr
NM_080722.4:c.3014G>A MANE Select NP_542453.2:p.Cys1005Tyr
NM_139155.3:c.3023G>A NP_631894.2:p.Cys1008Tyr
XM_011539300.2:c.2513G>A XP_011537602.1:p.Cys838Tyr
XM_011539301.2:c.2087G>A XP_011537603.1:p.Cys696Tyr
XM_011539302.2:c.2087G>A XP_011537604.1:p.Cys696Tyr
XM_011539308.2:c.*93G>A XP_011537610.1:n.*93G>A