Canonical Allele Identifier: CA2609525815

Gene: ADAMTS14

Linked Data

• gnomAD v4: 10-70757900-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70757905_70757907del , CM000672.2:g.70757905_70757907del	GRCh38
NC_000010.10:g.72517661_72517663del , CM000672.1:g.72517661_72517663del	GRCh37
NC_000010.9:g.72187667_72187669del	NCBI36
NG_042147.1:g.90103_90105del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2938-57_2938-55del MANE Select	ENSP00000362303.1:n.2938-57_2938-55del
ENST00000373207.1:c.2938-57_2938-55del	ENSP00000362303.1:n.2938-57_2938-55del
ENST00000373208.5:c.2947-57_2947-55del	ENSP00000362304.1:n.2947-57_2947-55del
NM_080722.3:c.2938-57_2938-55del	NP_542453.2:n.2938-57_2938-55del
NM_139155.2:c.2947-57_2947-55del	NP_631894.2:n.2947-57_2947-55del
XM_011539300.1:c.2437-57_2437-55del	XP_011537602.1:n.2437-57_2437-55del
XM_011539301.1:c.2011-57_2011-55del	XP_011537603.1:n.2011-57_2011-55del
XM_011539302.1:c.2011-57_2011-55del	XP_011537604.1:n.2011-57_2011-55del
XM_011539308.1:c.*17-57_*17-55del	XP_011537610.1:n.*17-57_*17-55del
XM_011539309.1:c.1507-57_1507-55del	XP_011537611.1:n.1507-57_1507-55del
NM_080722.4:c.2938-57_2938-55del MANE Select	NP_542453.2:n.2938-57_2938-55del
NM_139155.3:c.2947-57_2947-55del	NP_631894.2:n.2947-57_2947-55del
XM_011539300.2:c.2437-57_2437-55del	XP_011537602.1:n.2437-57_2437-55del
XM_011539301.2:c.2011-57_2011-55del	XP_011537603.1:n.2011-57_2011-55del
XM_011539302.2:c.2011-57_2011-55del	XP_011537604.1:n.2011-57_2011-55del
XM_011539308.2:c.*17-57_*17-55del	XP_011537610.1:n.*17-57_*17-55del