Canonical Allele Identifier: CA2647814626
Gene: ADAMTSL4 HGNC NCBI
ADAMTSL4-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150554187_150554188insAAGACCCAGCTTCA , CM000663.2:g.150554187_150554188insAAGACCCAGCTTCA GRCh38
NC_000001.10:g.150526663_150526664insAAGACCCAGCTTCA , CM000663.1:g.150526663_150526664insAAGACCCAGCTTCA GRCh37
NC_000001.9:g.148793287_148793288insAAGACCCAGCTTCA NCBI36
NG_012172.1:g.9766_9767insAAGACCCAGCTTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000271643.9:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) MANE Select ENSP00000271643.4:n.1131+65_1131+66insAAGACCCAGCTTCA
ENST00000674043.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) ENSP00000501295.1:n.1131+65_1131+66insAAGACCCAGCTTCA
ENST00000674058.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) ENSP00000501255.1:n.1131+65_1131+66insAAGACCCAGCTTCA
ENST00000271643.8:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) ENSP00000271643.4:n.1131+65_1131+66insAAGACCCAGCTTCA
ENST00000369038.6:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) ENSP00000358034.2:n.1131+65_1131+66insAAGACCCAGCTTCA
ENST00000369039.9:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) ENSP00000358035.5:n.1131+65_1131+66insAAGACCCAGCTTCA
ENST00000369041.9:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) ENSP00000358037.5:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_001288607.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_001275536.1:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_001288608.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_001275537.1:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_019032.5:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_061905.2:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_025008.4:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_079284.2:n.1131+65_1131+66insAAGACCCAGCTTCA
XM_011509644.1:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507946.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XM_011509645.1:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507947.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XM_011509646.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507948.1:n.1131+65_1131+66insAAGACCCAGCTTCA
XM_011509647.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507949.1:n.1131+65_1131+66insAAGACCCAGCTTCA
XM_011509648.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507950.1:n.1131+65_1131+66insAAGACCCAGCTTCA
XM_011509649.1:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507951.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XM_011509650.1:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507952.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XR_921844.1:n.1415+65_1415+66insAAGACCCAGCTTCA (ADAMTSL4)
XR_922132.1:n.370+347_370+348insTGAAGCTGGGTCTT (ADAMTSL4-AS2)
XR_922133.1:n.417+347_417+348insTGAAGCTGGGTCTT (ADAMTSL4-AS2)
XM_011509644.3:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507946.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XM_011509645.3:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507947.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XM_011509648.3:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507950.1:n.1131+65_1131+66insAAGACCCAGCTTCA
XM_011509649.3:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507951.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XM_011509650.3:c.1230+65_1230+66insAAGACCCAGCTTCA (ADAMTSL4) XP_011507952.1:n.1230+65_1230+66insAAGACCCAGCTTCA
XM_011509651.2:c.-335_-334insAAGACCCAGCTTCA (ADAMTSL4) XP_011507953.1:n.-335_-334insAAGACCCAGCTTCA
XM_017001506.2:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) XP_016856995.1:n.1131+65_1131+66insAAGACCCAGCTTCA
XR_001737242.2:n.1388+65_1388+66insAAGACCCAGCTTCA (ADAMTSL4)
XR_001738226.1:n.466+347_466+348insTGAAGCTGGGTCTT (ADAMTSL4-AS2)
XR_001738227.1:n.466+347_466+348insTGAAGCTGGGTCTT (ADAMTSL4-AS2)
XR_001738228.1:n.371+347_371+348insTGAAGCTGGGTCTT (ADAMTSL4-AS2)
XR_001738229.1:n.357+1766_357+1767insTGAAGCTGGGTCTT (ADAMTSL4-AS2)
XR_921844.3:n.1388+65_1388+66insAAGACCCAGCTTCA (ADAMTSL4)
NM_001288607.2:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_001275536.1:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_025008.5:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_079284.2:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_001288608.2:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_001275537.1:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_001378596.1:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) NP_001365525.1:n.1131+65_1131+66insAAGACCCAGCTTCA
NM_019032.6:c.1131+65_1131+66insAAGACCCAGCTTCA (ADAMTSL4) MANE Select NP_061905.2:n.1131+65_1131+66insAAGACCCAGCTTCA