Canonical Allele Identifier: CA470056245

Gene: ADAMTS14

Linked Data

• MyVariant Identifiers: chr10:g.72517810A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758054A>T , CM000672.2:g.70758054A>T	GRCh38
NC_000010.10:g.72517810A>T , CM000672.1:g.72517810A>T	GRCh37
NC_000010.9:g.72187816A>T	NCBI36
NG_042147.1:g.90252A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3030A>T MANE Select	ENSP00000362303.1:p.Pro1010=
ENST00000373207.1:c.3030A>T	ENSP00000362303.1:p.Pro1010=
ENST00000373208.5:c.3039A>T	ENSP00000362304.1:p.Pro1013=
NM_080722.3:c.3030A>T	NP_542453.2:p.Pro1010=
NM_139155.2:c.3039A>T	NP_631894.2:p.Pro1013=
XM_011539300.1:c.2529A>T	XP_011537602.1:p.Pro843=
XM_011539301.1:c.2103A>T	XP_011537603.1:p.Pro701=
XM_011539302.1:c.2103A>T	XP_011537604.1:p.Pro701=
XM_011539309.1:c.1599A>T	XP_011537611.1:p.Pro533=
NM_080722.4:c.3030A>T MANE Select	NP_542453.2:p.Pro1010=
NM_139155.3:c.3039A>T	NP_631894.2:p.Pro1013=
XM_011539300.2:c.2529A>T	XP_011537602.1:p.Pro843=
XM_011539301.2:c.2103A>T	XP_011537603.1:p.Pro701=
XM_011539302.2:c.2103A>T	XP_011537604.1:p.Pro701=