Canonical Allele Identifier: CA377108930
Gene: ADAMTS14 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000373207.2:c.3014G>T MANE Select ENSP00000362303.1:p.Cys1005Phe
ENST00000373207.1:c.3014G>T ENSP00000362303.1:p.Cys1005Phe
ENST00000373208.5:c.3023G>T ENSP00000362304.1:p.Cys1008Phe
NM_080722.3:c.3014G>T NP_542453.2:p.Cys1005Phe
NM_139155.2:c.3023G>T NP_631894.2:p.Cys1008Phe
XM_011539300.1:c.2513G>T XP_011537602.1:p.Cys838Phe
XM_011539301.1:c.2087G>T XP_011537603.1:p.Cys696Phe
XM_011539302.1:c.2087G>T XP_011537604.1:p.Cys696Phe
XM_011539309.1:c.1583G>T XP_011537611.1:p.Cys528Phe
NM_080722.4:c.3014G>T MANE Select NP_542453.2:p.Cys1005Phe
NM_139155.3:c.3023G>T NP_631894.2:p.Cys1008Phe
XM_011539300.2:c.2513G>T XP_011537602.1:p.Cys838Phe
XM_011539301.2:c.2087G>T XP_011537603.1:p.Cys696Phe
XM_011539302.2:c.2087G>T XP_011537604.1:p.Cys696Phe
XM_011539308.2:c.*93G>T XP_011537610.1:n.*93G>T