Canonical Allele Identifier: CA357430783

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179436C>G (hg19) ; chr4:g.72313719C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313719C>G , CM000666.2:g.72313719C>G	GRCh38
NC_000004.11:g.73179436C>G , CM000666.1:g.73179436C>G	GRCh37
NC_000004.10:g.73398300C>G	NCBI36
NG_046955.1:g.260081G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1703G>C MANE Select	ENSP00000286657.4:p.Gly568Ala
ENST00000286657.8:c.1703G>C	ENSP00000286657.4:p.Gly568Ala
ENST00000622135.1:c.1703G>C	ENSP00000480055.1:p.Gly568Ala
NM_014243.2:c.1703G>C	NP_055058.2:p.Gly568Ala
XM_011532421.1:c.1646G>C	XP_011530723.1:p.Gly549Ala
XM_011532422.1:c.1619G>C	XP_011530724.1:p.Gly540Ala
XM_011532423.1:c.1061G>C	XP_011530725.1:p.Gly354Ala
XM_011532424.1:c.971G>C	XP_011530726.1:p.Gly324Ala
XM_011532421.2:c.1646G>C	XP_011530723.1:p.Gly549Ala
XM_011532422.3:c.1619G>C	XP_011530724.1:p.Gly540Ala
NM_014243.3:c.1703G>C MANE Select	NP_055058.2:p.Gly568Ala