Canonical Allele Identifier: CA357430705

Gene: ADAMTS3

Linked Data

• MyVariant Identifiers: chr4:g.73179398G>A (hg19) ; chr4:g.72313681G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72313681G>A , CM000666.2:g.72313681G>A	GRCh38
NC_000004.11:g.73179398G>A , CM000666.1:g.73179398G>A	GRCh37
NC_000004.10:g.73398262G>A	NCBI36
NG_046955.1:g.260119C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.1741C>T MANE Select	ENSP00000286657.4:p.Pro581Ser
ENST00000286657.8:c.1741C>T	ENSP00000286657.4:p.Pro581Ser
ENST00000622135.1:c.1741C>T	ENSP00000480055.1:p.Pro581Ser
NM_014243.2:c.1741C>T	NP_055058.2:p.Pro581Ser
XM_011532421.1:c.1684C>T	XP_011530723.1:p.Pro562Ser
XM_011532422.1:c.1657C>T	XP_011530724.1:p.Pro553Ser
XM_011532423.1:c.1099C>T	XP_011530725.1:p.Pro367Ser
XM_011532424.1:c.1009C>T	XP_011530726.1:p.Pro337Ser
XM_011532421.2:c.1684C>T	XP_011530723.1:p.Pro562Ser
XM_011532422.3:c.1657C>T	XP_011530724.1:p.Pro553Ser
NM_014243.3:c.1741C>T MANE Select	NP_055058.2:p.Pro581Ser