Canonical Allele Identifier: CA2574053762
Gene: ADAMTSL4 HGNC NCBI
ADAMTSL4-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150557147_150557148del , CM000663.2:g.150557147_150557148del GRCh38
NC_000001.10:g.150529623_150529624del , CM000663.1:g.150529623_150529624del GRCh37
NC_000001.9:g.148796247_148796248del NCBI36
NG_012172.1:g.12726_12727del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271643.9:c.1862-3_1862-2del (ADAMTSL4) MANE Select ENSP00000271643.4:n.1862-3_1862-2del
ENST00000674043.1:c.1931-3_1931-2del (ADAMTSL4) ENSP00000501295.1:n.1931-3_1931-2del
ENST00000674058.1:c.1857-115_1857-114del (ADAMTSL4) ENSP00000501255.1:n.1857-115_1857-114del
ENST00000271643.8:c.1862-3_1862-2del (ADAMTSL4) ENSP00000271643.4:n.1862-3_1862-2del
ENST00000369038.6:c.1862-3_1862-2del (ADAMTSL4) ENSP00000358034.2:n.1862-3_1862-2del
ENST00000369039.9:c.1931-3_1931-2del (ADAMTSL4) ENSP00000358035.5:n.1931-3_1931-2del
ENST00000369041.9:c.1862-3_1862-2del (ADAMTSL4) ENSP00000358037.5:n.1862-3_1862-2del
ENST00000622417.4:c.476-3_476-2del (ADAMTSL4) ENSP00000477897.1:n.476-3_476-2del
NM_001288607.1:c.1857-115_1857-114del (ADAMTSL4) NP_001275536.1:n.1857-115_1857-114del
NM_001288608.1:c.1931-3_1931-2del (ADAMTSL4) NP_001275537.1:n.1931-3_1931-2del
NM_019032.5:c.1862-3_1862-2del (ADAMTSL4) NP_061905.2:n.1862-3_1862-2del
NM_025008.4:c.1862-3_1862-2del (ADAMTSL4) NP_079284.2:n.1862-3_1862-2del
XM_011509644.1:c.2030-3_2030-2del (ADAMTSL4) XP_011507946.1:n.2030-3_2030-2del
XM_011509645.1:c.1961-3_1961-2del (ADAMTSL4) XP_011507947.1:n.1961-3_1961-2del
XM_011509646.1:c.1931-3_1931-2del (ADAMTSL4) XP_011507948.1:n.1931-3_1931-2del
XM_011509647.1:c.1931-3_1931-2del (ADAMTSL4) XP_011507949.1:n.1931-3_1931-2del
XM_011509648.1:c.1931-3_1931-2del (ADAMTSL4) XP_011507950.1:n.1931-3_1931-2del
XM_011509649.1:c.2030-3_2030-2del (ADAMTSL4) XP_011507951.1:n.2030-3_2030-2del
XM_011509650.1:c.2030-3_2030-2del (ADAMTSL4) XP_011507952.1:n.2030-3_2030-2del
XM_011509651.1:c.539-3_539-2del (ADAMTSL4) XP_011507953.1:n.539-3_539-2del
XM_011509652.1:c.539-3_539-2del (ADAMTSL4) XP_011507954.1:n.539-3_539-2del
XR_921844.1:n.2215-3_2215-2del (ADAMTSL4)
XR_922133.1:n.139+547_139+548del (ADAMTSL4-AS2)
XM_011509644.3:c.2030-3_2030-2del (ADAMTSL4) XP_011507946.1:n.2030-3_2030-2del
XM_011509645.3:c.1961-3_1961-2del (ADAMTSL4) XP_011507947.1:n.1961-3_1961-2del
XM_011509648.3:c.1931-3_1931-2del (ADAMTSL4) XP_011507950.1:n.1931-3_1931-2del
XM_011509649.3:c.2030-3_2030-2del (ADAMTSL4) XP_011507951.1:n.2030-3_2030-2del
XM_011509650.3:c.2030-3_2030-2del (ADAMTSL4) XP_011507952.1:n.2030-3_2030-2del
XM_011509651.2:c.539-3_539-2del (ADAMTSL4) XP_011507953.1:n.539-3_539-2del
XM_011509652.2:c.539-3_539-2del (ADAMTSL4) XP_011507954.1:n.539-3_539-2del
XM_017001506.2:c.1931-3_1931-2del (ADAMTSL4) XP_016856995.1:n.1931-3_1931-2del
XM_017001507.1:c.275-3_275-2del (ADAMTSL4) XP_016856996.1:n.275-3_275-2del
XR_001737242.2:n.2015-3_2015-2del (ADAMTSL4)
XR_921844.3:n.2188-3_2188-2del (ADAMTSL4)
NM_001288607.2:c.1857-115_1857-114del (ADAMTSL4) NP_001275536.1:n.1857-115_1857-114del
NM_025008.5:c.1862-3_1862-2del (ADAMTSL4) NP_079284.2:n.1862-3_1862-2del
NM_001288608.2:c.1931-3_1931-2del (ADAMTSL4) NP_001275537.1:n.1931-3_1931-2del
NM_001378596.1:c.1862-3_1862-2del (ADAMTSL4) NP_001365525.1:n.1862-3_1862-2del
NM_019032.6:c.1862-3_1862-2del (ADAMTSL4) MANE Select NP_061905.2:n.1862-3_1862-2del