Canonical Allele Identifier: CA396832429

Gene: ADAMTS18

Linked Data

• MyVariant Identifiers: chr16:g.77369785T>G (hg19) ; chr16:g.77335888T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335888T>G , CM000678.2:g.77335888T>G	GRCh38
NC_000016.9:g.77369785T>G , CM000678.1:g.77369785T>G	GRCh37
NC_000016.8:g.75927286T>G	NCBI36
NG_031879.1:g.104227A>C
NG_031879.2:g.104227A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.1727A>C MANE Select	ENSP00000282849.5:p.Gln576Pro
ENST00000282849.9:c.1727A>C	ENSP00000282849.5:p.Gln576Pro
NM_199355.2:c.1727A>C	NP_955387.1:p.Gln576Pro
XM_011522923.1:c.1211A>C	XP_011521225.1:p.Gln404Pro
XM_011522924.1:c.1211A>C	XP_011521226.1:p.Gln404Pro
NM_001326358.1:c.1211A>C	NP_001313287.1:p.Gln404Pro
NM_199355.3:c.1727A>C	NP_955387.1:p.Gln576Pro
XM_011522924.2:c.1211A>C	XP_011521226.1:p.Gln404Pro
XM_017022988.2:c.491A>C	XP_016878477.1:p.Gln164Pro
XM_017022989.1:c.491A>C	XP_016878478.1:p.Gln164Pro
NM_199355.4:c.1727A>C MANE Select	NP_955387.1:p.Gln576Pro
NM_001326358.2:c.1211A>C	NP_001313287.1:p.Gln404Pro