Canonical Allele Identifier: CA284411762

Gene: ADAMTS18

Linked Data

• dbSNP Id: rs773263590
• gnomAD v2: 16-77428901-G-A
• gnomAD v3: 16-77395004-G-A
• gnomAD v4: 16-77395004-G-A
• MyVariant Identifiers: chr16:g.77428901G>A (hg19) ; chr16:g.77395004G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77395004G>A , CM000678.2:g.77395004G>A	GRCh38
NC_000016.9:g.77428901G>A , CM000678.1:g.77428901G>A	GRCh37
NC_000016.8:g.75986402G>A	NCBI36
NG_031879.1:g.45111C>T
NG_031879.2:g.45111C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282849.10:c.496-27281C>T MANE Select	ENSP00000282849.5:n.496-27281C>T
ENST00000282849.9:c.496-27281C>T	ENSP00000282849.5:n.496-27281C>T
ENST00000449265.2:c.496-27281C>T	ENSP00000392540.2:n.496-27281C>T
ENST00000562345.1:c.294-27335C>T
ENST00000564369.1:n.422-27281C>T
ENST00000567121.5:n.353-27281C>T
ENST00000567914.1:n.340-27281C>T
ENST00000569309.1:n.453-16025C>T
NM_199355.2:c.496-27281C>T	NP_955387.1:n.496-27281C>T
XM_011522923.1:c.-25-27281C>T	XP_011521225.1:n.-25-27281C>T
XM_011522924.1:c.-25-27281C>T	XP_011521226.1:n.-25-27281C>T
NM_001326358.1:c.-25-27281C>T	NP_001313287.1:n.-25-27281C>T
NM_199355.3:c.496-27281C>T	NP_955387.1:n.496-27281C>T
XM_011522924.2:c.-25-27281C>T	XP_011521226.1:n.-25-27281C>T
XM_017022988.2:c.-585-27281C>T	XP_016878477.1:n.-585-27281C>T
XM_017022989.1:c.-581-27281C>T	XP_016878478.1:n.-581-27281C>T
NM_199355.4:c.496-27281C>T MANE Select	NP_955387.1:n.496-27281C>T
NM_001326358.2:c.-25-27281C>T	NP_001313287.1:n.-25-27281C>T