Canonical Allele Identifier: CA14137055
Gene: ADAMTSL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.83911830A>C , CM000677.2:g.83911830A>C GRCh38
NC_000015.9:g.84580582A>C , CM000677.1:g.84580582A>C GRCh37
NC_000015.8:g.82371586A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286744.10:c.1701-1262A>C MANE Select ENSP00000286744.5:n.1701-1262A>C
ENST00000286744.9:c.1701-1262A>C ENSP00000286744.5:n.1701-1262A>C
ENST00000561483.5:n.1916-1262A>C
ENST00000567476.1:c.1701-1262A>C ENSP00000456313.1:n.1701-1262A>C
NM_001301110.1:c.1701-1262A>C NP_001288039.1:n.1701-1262A>C
NM_207517.2:c.1701-1262A>C NP_997400.2:n.1701-1262A>C
XM_011521821.1:c.1782-1262A>C XP_011520123.1:n.1782-1262A>C
XM_011521822.1:c.1782-1262A>C XP_011520124.1:n.1782-1262A>C
XM_011521823.1:c.1782-1262A>C XP_011520125.1:n.1782-1262A>C
XM_011521824.1:c.1782-1262A>C XP_011520126.1:n.1782-1262A>C
XM_011521825.1:c.1782-1262A>C XP_011520127.1:n.1782-1262A>C
XR_931873.1:n.1815-1262A>C
XM_011521822.2:c.1782-1262A>C XP_011520124.1:n.1782-1262A>C
XM_011521823.2:c.1782-1262A>C XP_011520125.1:n.1782-1262A>C
XM_011521824.2:c.1782-1262A>C XP_011520126.1:n.1782-1262A>C
XM_011521825.2:c.1782-1262A>C XP_011520127.1:n.1782-1262A>C
XM_017022434.1:c.1782-1262A>C XP_016877923.1:n.1782-1262A>C
XM_017022435.1:c.1206-1262A>C XP_016877924.1:n.1206-1262A>C
XM_024450000.1:c.1782-1262A>C XP_024305768.1:n.1782-1262A>C
XR_931873.2:n.1997-1262A>C
NM_207517.3:c.1701-1262A>C MANE Select NP_997400.2:n.1701-1262A>C
NM_001301110.2:c.1701-1262A>C NP_001288039.1:n.1701-1262A>C