Canonical Allele Identifier: CA377108956

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517806G>T (hg19) ; chr10:g.70758050G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758050G>T , CM000672.2:g.70758050G>T	GRCh38
NC_000010.10:g.72517806G>T , CM000672.1:g.72517806G>T	GRCh37
NC_000010.9:g.72187812G>T	NCBI36
NG_042147.1:g.90248G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3026G>T MANE Select	ENSP00000362303.1:p.Arg1009Met
ENST00000373207.1:c.3026G>T	ENSP00000362303.1:p.Arg1009Met
ENST00000373208.5:c.3035G>T	ENSP00000362304.1:p.Arg1012Met
NM_080722.3:c.3026G>T	NP_542453.2:p.Arg1009Met
NM_139155.2:c.3035G>T	NP_631894.2:p.Arg1012Met
XM_011539300.1:c.2525G>T	XP_011537602.1:p.Arg842Met
XM_011539301.1:c.2099G>T	XP_011537603.1:p.Arg700Met
XM_011539302.1:c.2099G>T	XP_011537604.1:p.Arg700Met
XM_011539309.1:c.1595G>T	XP_011537611.1:p.Arg532Met
NM_080722.4:c.3026G>T MANE Select	NP_542453.2:p.Arg1009Met
NM_139155.3:c.3035G>T	NP_631894.2:p.Arg1012Met
XM_011539300.2:c.2525G>T	XP_011537602.1:p.Arg842Met
XM_011539301.2:c.2099G>T	XP_011537603.1:p.Arg700Met
XM_011539302.2:c.2099G>T	XP_011537604.1:p.Arg700Met