Canonical Allele Identifier: CA209416011

Gene: ADAMTS14

Linked Data

• dbSNP Id: rs752461017
• gnomAD v4: 10-70758079-C-A
• MyVariant Identifiers: chr10:g.72517835C>A (hg19) ; chr10:g.70758079C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758079C>A , CM000672.2:g.70758079C>A	GRCh38
NC_000010.10:g.72517835C>A , CM000672.1:g.72517835C>A	GRCh37
NC_000010.9:g.72187841C>A	NCBI36
NG_042147.1:g.90277C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3055C>A MANE Select	ENSP00000362303.1:p.Pro1019Thr
ENST00000373207.1:c.3055C>A	ENSP00000362303.1:p.Pro1019Thr
ENST00000373208.5:c.3064C>A	ENSP00000362304.1:p.Pro1022Thr
NM_080722.3:c.3055C>A	NP_542453.2:p.Pro1019Thr
NM_139155.2:c.3064C>A	NP_631894.2:p.Pro1022Thr
XM_011539300.1:c.2554C>A	XP_011537602.1:p.Pro852Thr
XM_011539301.1:c.2128C>A	XP_011537603.1:p.Pro710Thr
XM_011539302.1:c.2128C>A	XP_011537604.1:p.Pro710Thr
XM_011539309.1:c.1624C>A	XP_011537611.1:p.Pro542Thr
NM_080722.4:c.3055C>A MANE Select	NP_542453.2:p.Pro1019Thr
NM_139155.3:c.3064C>A	NP_631894.2:p.Pro1022Thr
XM_011539300.2:c.2554C>A	XP_011537602.1:p.Pro852Thr
XM_011539301.2:c.2128C>A	XP_011537603.1:p.Pro710Thr
XM_011539302.2:c.2128C>A	XP_011537604.1:p.Pro710Thr