Canonical Allele Identifier: CA377109083

Gene: ADAMTS14

Linked Data

• gnomAD v4: 10-70758187-A-T
• MyVariant Identifiers: chr10:g.72517943A>T (hg19) ; chr10:g.70758187A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70758187A>T , CM000672.2:g.70758187A>T	GRCh38
NC_000010.10:g.72517943A>T , CM000672.1:g.72517943A>T	GRCh37
NC_000010.9:g.72187949A>T	NCBI36
NG_042147.1:g.90385A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000373207.2:c.3080A>T MANE Select	ENSP00000362303.1:p.Asn1027Ile
ENST00000373207.1:c.3080A>T	ENSP00000362303.1:p.Asn1027Ile
ENST00000373208.5:c.3089A>T	ENSP00000362304.1:p.Asn1030Ile
NM_080722.3:c.3080A>T	NP_542453.2:p.Asn1027Ile
NM_139155.2:c.3089A>T	NP_631894.2:p.Asn1030Ile
XM_011539300.1:c.2579A>T	XP_011537602.1:p.Asn860Ile
XM_011539301.1:c.2153A>T	XP_011537603.1:p.Asn718Ile
XM_011539302.1:c.2153A>T	XP_011537604.1:p.Asn718Ile
XM_011539309.1:c.1649A>T	XP_011537611.1:p.Asn550Ile
NM_080722.4:c.3080A>T MANE Select	NP_542453.2:p.Asn1027Ile
NM_139155.3:c.3089A>T	NP_631894.2:p.Asn1030Ile
XM_011539300.2:c.2579A>T	XP_011537602.1:p.Asn860Ile
XM_011539301.2:c.2153A>T	XP_011537603.1:p.Asn718Ile
XM_011539302.2:c.2153A>T	XP_011537604.1:p.Asn718Ile