Canonical Allele Identifier: CA396831867

Gene: ADAMTS18

Linked Data

• gnomAD v4: 16-77335787-T-A
• MyVariant Identifiers: chr16:g.77369684T>A (hg19) ; chr16:g.77335787T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.77335787T>A , CM000678.2:g.77335787T>A	GRCh38
NC_000016.9:g.77369684T>A , CM000678.1:g.77369684T>A	GRCh37
NC_000016.8:g.75927185T>A	NCBI36
NG_031879.1:g.104328A>T
NG_031879.2:g.104328A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282849.10:c.1828A>T MANE Select	ENSP00000282849.5:p.Lys610Ter
ENST00000282849.9:c.1828A>T	ENSP00000282849.5:p.Lys610Ter
NM_199355.2:c.1828A>T	NP_955387.1:p.Lys610Ter
XM_006721158.2:c.-88A>T	XP_006721221.1:n.-88A>T
XM_011522923.1:c.1312A>T	XP_011521225.1:p.Lys438Ter
XM_011522924.1:c.1312A>T	XP_011521226.1:p.Lys438Ter
NM_001326358.1:c.1312A>T	NP_001313287.1:p.Lys438Ter
NM_199355.3:c.1828A>T	NP_955387.1:p.Lys610Ter
XM_011522924.2:c.1312A>T	XP_011521226.1:p.Lys438Ter
XM_017022988.2:c.592A>T	XP_016878477.1:p.Lys198Ter
XM_017022989.1:c.592A>T	XP_016878478.1:p.Lys198Ter
NM_199355.4:c.1828A>T MANE Select	NP_955387.1:p.Lys610Ter
NM_001326358.2:c.1312A>T	NP_001313287.1:p.Lys438Ter