Canonical Allele Identifier: CA2578109973
Gene: ADAMTS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.72313637G>A , CM000666.2:g.72313637G>A GRCh38
NC_000004.11:g.73179354G>A , CM000666.1:g.73179354G>A GRCh37
NC_000004.10:g.73398218G>A NCBI36
NG_046955.1:g.260163C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286657.10:c.1745+40C>T MANE Select ENSP00000286657.4:n.1745+40C>T
ENST00000286657.8:c.1745+40C>T ENSP00000286657.4:n.1745+40C>T
ENST00000622135.1:c.1745+40C>T ENSP00000480055.1:n.1745+40C>T
NM_014243.2:c.1745+40C>T NP_055058.2:n.1745+40C>T
XM_011532421.1:c.1688+40C>T XP_011530723.1:n.1688+40C>T
XM_011532422.1:c.1661+40C>T XP_011530724.1:n.1661+40C>T
XM_011532423.1:c.1103+40C>T XP_011530725.1:n.1103+40C>T
XM_011532424.1:c.1013+40C>T XP_011530726.1:n.1013+40C>T
XM_011532421.2:c.1688+40C>T XP_011530723.1:n.1688+40C>T
XM_011532422.3:c.1661+40C>T XP_011530724.1:n.1661+40C>T
NM_014243.3:c.1745+40C>T MANE Select NP_055058.2:n.1745+40C>T