Canonical Allele Identifier: CA2838206458

Gene: ADAMTS3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.72331414T>C , CM000666.2:g.72331414T>C	GRCh38
NC_000004.11:g.73197131T>C , CM000666.1:g.73197131T>C	GRCh37
NC_000004.10:g.73415995T>C	NCBI36
NG_046955.1:g.242386A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000286657.10:c.861+8080A>G MANE Select	ENSP00000286657.4:n.861+8080A>G
ENST00000286657.8:c.861+8080A>G	ENSP00000286657.4:n.861+8080A>G
ENST00000622135.1:c.861+8080A>G	ENSP00000480055.1:n.861+8080A>G
NM_014243.2:c.861+8080A>G	NP_055058.2:n.861+8080A>G
XM_011532421.1:c.804+8080A>G	XP_011530723.1:n.804+8080A>G
XM_011532422.1:c.777+8080A>G	XP_011530724.1:n.777+8080A>G
XM_011532423.1:c.219+8080A>G	XP_011530725.1:n.219+8080A>G
XM_011532424.1:c.129+8080A>G	XP_011530726.1:n.129+8080A>G
XM_011532421.2:c.804+8080A>G	XP_011530723.1:n.804+8080A>G
XM_011532422.3:c.777+8080A>G	XP_011530724.1:n.777+8080A>G
NM_014243.3:c.861+8080A>G MANE Select	NP_055058.2:n.861+8080A>G