Canonical Allele Identifier: CA396831978

Gene: ADAMTS18

Linked Data

• MyVariant Identifiers: chr16:g.77369702T>G (hg19) ; chr16:g.77335805T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335805T>G , CM000678.2:g.77335805T>G	GRCh38
NC_000016.9:g.77369702T>G , CM000678.1:g.77369702T>G	GRCh37
NC_000016.8:g.75927203T>G	NCBI36
NG_031879.1:g.104310A>C
NG_031879.2:g.104310A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282849.10:c.1810A>C MANE Select	ENSP00000282849.5:p.Thr604Pro
ENST00000282849.9:c.1810A>C	ENSP00000282849.5:p.Thr604Pro
NM_199355.2:c.1810A>C	NP_955387.1:p.Thr604Pro
XM_006721158.2:c.-106A>C	XP_006721221.1:n.-106A>C
XM_011522923.1:c.1294A>C	XP_011521225.1:p.Thr432Pro
XM_011522924.1:c.1294A>C	XP_011521226.1:p.Thr432Pro
NM_001326358.1:c.1294A>C	NP_001313287.1:p.Thr432Pro
NM_199355.3:c.1810A>C	NP_955387.1:p.Thr604Pro
XM_011522924.2:c.1294A>C	XP_011521226.1:p.Thr432Pro
XM_017022988.2:c.574A>C	XP_016878477.1:p.Thr192Pro
XM_017022989.1:c.574A>C	XP_016878478.1:p.Thr192Pro
NM_199355.4:c.1810A>C MANE Select	NP_955387.1:p.Thr604Pro
NM_001326358.2:c.1294A>C	NP_001313287.1:p.Thr432Pro