Canonical Allele Identifier: CA2609525998

Gene: ADAMTS14

Linked Data

• gnomAD v4: 10-70758004-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758005del , CM000672.2:g.70758005del	GRCh38
NC_000010.10:g.72517761del , CM000672.1:g.72517761del	GRCh37
NC_000010.9:g.72187767del	NCBI36
NG_042147.1:g.90203del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.2981del MANE Select	ENSP00000362303.1:p.Val994GlyfsTer?
ENST00000373207.1:c.2981del	ENSP00000362303.1:p.Val994GlyfsTer?
ENST00000373208.5:c.2990del	ENSP00000362304.1:p.Val997GlyfsTer?
NM_080722.3:c.2981del	NP_542453.2:p.Val994GlyfsTer?
NM_139155.2:c.2990del	NP_631894.2:p.Val997GlyfsTer?
XM_011539300.1:c.2480del	XP_011537602.1:p.Val827GlyfsTer?
XM_011539301.1:c.2054del	XP_011537603.1:p.Val685GlyfsTer?
XM_011539302.1:c.2054del	XP_011537604.1:p.Val685GlyfsTer?
XM_011539308.1:c.*60del	XP_011537610.1:n.*60del
XM_011539309.1:c.1550del	XP_011537611.1:p.Val517GlyfsTer?
NM_080722.4:c.2981del MANE Select	NP_542453.2:p.Val994GlyfsTer?
NM_139155.3:c.2990del	NP_631894.2:p.Val997GlyfsTer?
XM_011539300.2:c.2480del	XP_011537602.1:p.Val827GlyfsTer?
XM_011539301.2:c.2054del	XP_011537603.1:p.Val685GlyfsTer?
XM_011539302.2:c.2054del	XP_011537604.1:p.Val685GlyfsTer?
XM_011539308.2:c.*60del	XP_011537610.1:n.*60del