Canonical Allele Identifier: CA2746063811
Gene: ADAMTSL4 HGNC NCBI
ADAMTSL4-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.150557012del , CM000663.2:g.150557012del GRCh38
NC_000001.10:g.150529488del , CM000663.1:g.150529488del GRCh37
NC_000001.9:g.148796112del NCBI36
NG_012172.1:g.12591del

Transcript Alleles

HGVS Amino-acid Change
ENST00000271643.9:c.1823del (ADAMTSL4) MANE Select ENSP00000271643.4:p.Asn608ThrfsTer16
ENST00000674043.1:c.1892del (ADAMTSL4) ENSP00000501295.1:p.Asn631ThrfsTer16
ENST00000674058.1:c.1856+36del (ADAMTSL4) ENSP00000501255.1:n.1856+36del
ENST00000271643.8:c.1823del (ADAMTSL4) ENSP00000271643.4:p.Asn608ThrfsTer16
ENST00000369038.6:c.1823del (ADAMTSL4) ENSP00000358034.2:p.Asn608ThrfsTer16
ENST00000369039.9:c.1892del (ADAMTSL4) ENSP00000358035.5:p.Asn631ThrfsTer16
ENST00000369041.9:c.1823del (ADAMTSL4) ENSP00000358037.5:p.Asn608ThrfsTer16
ENST00000622417.4:c.437del (ADAMTSL4) ENSP00000477897.1:p.Asn146ThrfsTer16
NM_001288607.1:c.1856+36del (ADAMTSL4) NP_001275536.1:n.1856+36del
NM_001288608.1:c.1892del (ADAMTSL4) NP_001275537.1:p.Asn631ThrfsTer16
NM_019032.5:c.1823del (ADAMTSL4) NP_061905.2:p.Asn608ThrfsTer16
NM_025008.4:c.1823del (ADAMTSL4) NP_079284.2:p.Asn608ThrfsTer16
XM_011509644.1:c.1991del (ADAMTSL4) XP_011507946.1:p.Asn664ThrfsTer16
XM_011509645.1:c.1922del (ADAMTSL4) XP_011507947.1:p.Asn641ThrfsTer16
XM_011509646.1:c.1892del (ADAMTSL4) XP_011507948.1:p.Asn631ThrfsTer16
XM_011509647.1:c.1892del (ADAMTSL4) XP_011507949.1:p.Asn631ThrfsTer16
XM_011509648.1:c.1892del (ADAMTSL4) XP_011507950.1:p.Asn631ThrfsTer16
XM_011509649.1:c.1991del (ADAMTSL4) XP_011507951.1:p.Asn664ThrfsTer16
XM_011509650.1:c.1991del (ADAMTSL4) XP_011507952.1:p.Asn664ThrfsTer16
XM_011509651.1:c.500del (ADAMTSL4) XP_011507953.1:p.Asn167ThrfsTer16
XM_011509652.1:c.500del (ADAMTSL4) XP_011507954.1:p.Asn167ThrfsTer16
XR_921844.1:n.2176del (ADAMTSL4)
XR_922133.1:n.139+682del (ADAMTSL4-AS2)
XM_011509644.3:c.1991del (ADAMTSL4) XP_011507946.1:p.Asn664ThrfsTer16
XM_011509645.3:c.1922del (ADAMTSL4) XP_011507947.1:p.Asn641ThrfsTer16
XM_011509648.3:c.1892del (ADAMTSL4) XP_011507950.1:p.Asn631ThrfsTer16
XM_011509649.3:c.1991del (ADAMTSL4) XP_011507951.1:p.Asn664ThrfsTer16
XM_011509650.3:c.1991del (ADAMTSL4) XP_011507952.1:p.Asn664ThrfsTer16
XM_011509651.2:c.500del (ADAMTSL4) XP_011507953.1:p.Asn167ThrfsTer16
XM_011509652.2:c.500del (ADAMTSL4) XP_011507954.1:p.Asn167ThrfsTer16
XM_017001506.2:c.1892del (ADAMTSL4) XP_016856995.1:p.Asn631ThrfsTer16
XM_017001507.1:c.236del (ADAMTSL4) XP_016856996.1:p.Asn79ThrfsTer16
XR_001737242.2:n.1976del (ADAMTSL4)
XR_921844.3:n.2149del (ADAMTSL4)
NM_001288607.2:c.1856+36del (ADAMTSL4) NP_001275536.1:n.1856+36del
NM_025008.5:c.1823del (ADAMTSL4) NP_079284.2:p.Asn608ThrfsTer16
NM_001288608.2:c.1892del (ADAMTSL4) NP_001275537.1:p.Asn631ThrfsTer16
NM_001378596.1:c.1823del (ADAMTSL4) NP_001365525.1:p.Asn608ThrfsTer16
NM_019032.6:c.1823del (ADAMTSL4) MANE Select NP_061905.2:p.Asn608ThrfsTer16