Canonical Allele Identifier: CA377109054

Gene: ADAMTS14

Linked Data

• dbSNP Id: rs1450077759
• gnomAD v2: 10-72517933-A-C
• gnomAD v3: 10-70758177-A-C
• gnomAD v4: 10-70758177-A-C
• MyVariant Identifiers: chr10:g.72517933A>C (hg19) ; chr10:g.70758177A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758177A>C , CM000672.2:g.70758177A>C	GRCh38
NC_000010.10:g.72517933A>C , CM000672.1:g.72517933A>C	GRCh37
NC_000010.9:g.72187939A>C	NCBI36
NG_042147.1:g.90375A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3070A>C MANE Select	ENSP00000362303.1:p.Asn1024His
ENST00000373207.1:c.3070A>C	ENSP00000362303.1:p.Asn1024His
ENST00000373208.5:c.3079A>C	ENSP00000362304.1:p.Asn1027His
NM_080722.3:c.3070A>C	NP_542453.2:p.Asn1024His
NM_139155.2:c.3079A>C	NP_631894.2:p.Asn1027His
XM_011539300.1:c.2569A>C	XP_011537602.1:p.Asn857His
XM_011539301.1:c.2143A>C	XP_011537603.1:p.Asn715His
XM_011539302.1:c.2143A>C	XP_011537604.1:p.Asn715His
XM_011539309.1:c.1639A>C	XP_011537611.1:p.Asn547His
NM_080722.4:c.3070A>C MANE Select	NP_542453.2:p.Asn1024His
NM_139155.3:c.3079A>C	NP_631894.2:p.Asn1027His
XM_011539300.2:c.2569A>C	XP_011537602.1:p.Asn857His
XM_011539301.2:c.2143A>C	XP_011537603.1:p.Asn715His
XM_011539302.2:c.2143A>C	XP_011537604.1:p.Asn715His