Canonical Allele Identifier: CA1581900109
Gene: ADAMTS19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.129664693T>A , CM000667.2:g.129664693T>A GRCh38
NC_000005.9:g.129000386T>A , CM000667.1:g.129000386T>A GRCh37
NC_000005.8:g.129028285T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000274487.9:c.2426-806T>A MANE Select ENSP00000274487.5:n.2426-806T>A
ENST00000274487.8:c.2408-806T>A ENSP00000274487.4:n.2408-806T>A
NM_133638.3:c.2408-806T>A NP_598377.3:n.2408-806T>A
XM_011543246.1:c.1706-806T>A XP_011541548.1:n.1706-806T>A
XM_011543247.1:c.1235-806T>A XP_011541549.1:n.1235-806T>A
XM_011543248.1:c.1235-806T>A XP_011541550.1:n.1235-806T>A
XM_011543249.1:c.1094-806T>A XP_011541551.1:n.1094-806T>A
NM_133638.4:c.2426-806T>A NP_598377.4:n.2426-806T>A
XM_011543246.2:c.1706-806T>A XP_011541548.1:n.1706-806T>A
XM_011543247.2:c.1235-806T>A XP_011541549.1:n.1235-806T>A
XM_011543248.2:c.1235-806T>A XP_011541550.1:n.1235-806T>A
XM_011543249.2:c.1094-806T>A XP_011541551.1:n.1094-806T>A
XM_017009174.1:c.1412-806T>A XP_016864663.1:n.1412-806T>A
XM_017009175.1:c.1094-806T>A XP_016864664.1:n.1094-806T>A
XM_017009176.1:c.1082-806T>A XP_016864665.1:n.1082-806T>A
NM_133638.5:c.2426-806T>A NP_598377.4:n.2426-806T>A
NM_133638.6:c.2426-806T>A MANE Select NP_598377.4:n.2426-806T>A