Canonical Allele Identifier: CA668064663

Gene: ADAMTS14

Linked Data

• dbSNP Id: rs17600642
• gnomAD v3: 10-70703238-C-T
• gnomAD v4: 10-70703238-C-T
• MyVariant Identifiers: chr10:g.72462994C>T (hg19) ; chr10:g.70703238C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70703238C>T , CM000672.2:g.70703238C>T	GRCh38
NC_000010.10:g.72462994C>T , CM000672.1:g.72462994C>T	GRCh37
NC_000010.9:g.72133000C>T	NCBI36
NG_042147.1:g.35436C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000373207.2:c.679+770C>T MANE Select	ENSP00000362303.1:n.679+770C>T
ENST00000373207.1:c.679+770C>T	ENSP00000362303.1:n.679+770C>T
ENST00000373208.5:c.679+770C>T	ENSP00000362304.1:n.679+770C>T
NM_080722.3:c.679+770C>T	NP_542453.2:n.679+770C>T
NM_139155.2:c.679+770C>T	NP_631894.2:n.679+770C>T
XM_011539300.1:c.679+770C>T	XP_011537602.1:n.679+770C>T
XM_011539303.1:c.679+770C>T	XP_011537605.1:n.679+770C>T
XM_011539304.1:c.679+770C>T	XP_011537606.1:n.679+770C>T
XM_011539305.1:c.679+770C>T	XP_011537607.1:n.679+770C>T
XM_011539306.1:c.679+770C>T	XP_011537608.1:n.679+770C>T
XM_011539307.1:c.679+770C>T	XP_011537609.1:n.679+770C>T
XM_011539308.1:c.679+770C>T	XP_011537610.1:n.679+770C>T
NM_080722.4:c.679+770C>T MANE Select	NP_542453.2:n.679+770C>T
NM_139155.3:c.679+770C>T	NP_631894.2:n.679+770C>T
XM_011539300.2:c.679+770C>T	XP_011537602.1:n.679+770C>T
XM_011539303.2:c.679+770C>T	XP_011537605.1:n.679+770C>T
XM_011539306.2:c.679+770C>T	XP_011537608.1:n.679+770C>T
XM_011539307.2:c.679+770C>T	XP_011537609.1:n.679+770C>T
XM_011539308.2:c.679+770C>T	XP_011537610.1:n.679+770C>T
XR_001747025.1:n.964+770C>T