Canonical Allele Identifier: CA2479209028

Gene: ADAMTSL4 ADAMTSL4-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150553168_150553169delinsCA , CM000663.2:g.150553168_150553169delinsCA	GRCh38
NC_000001.10:g.150525644_150525645delinsCA , CM000663.1:g.150525644_150525645delinsCA	GRCh37
NC_000001.9:g.148792268_148792269delinsCA	NCBI36
NG_012172.1:g.8747_8748delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.349_350delinsCA (ADAMTSL4) MANE Select	ENSP00000271643.4:p.Gln117=
ENST00000674043.1:c.349_350delinsCA (ADAMTSL4)	ENSP00000501295.1:p.Gln117=
ENST00000674058.1:c.349_350delinsCA (ADAMTSL4)	ENSP00000501255.1:p.Gln117=
ENST00000271643.8:c.349_350delinsCA (ADAMTSL4)	ENSP00000271643.4:p.Gln117=
ENST00000369038.6:c.349_350delinsCA (ADAMTSL4)	ENSP00000358034.2:p.Gln117=
ENST00000369039.9:c.349_350delinsCA (ADAMTSL4)	ENSP00000358035.5:p.Gln117=
ENST00000369041.9:c.349_350delinsCA (ADAMTSL4)	ENSP00000358037.5:p.Gln117=
NM_001288607.1:c.349_350delinsCA (ADAMTSL4)	NP_001275536.1:p.Gln117=
NM_001288608.1:c.349_350delinsCA (ADAMTSL4)	NP_001275537.1:p.Gln117=
NM_019032.5:c.349_350delinsCA (ADAMTSL4)	NP_061905.2:p.Gln117=
NM_025008.4:c.349_350delinsCA (ADAMTSL4)	NP_079284.2:p.Gln117=
XM_011509644.1:c.448_449delinsCA (ADAMTSL4)	XP_011507946.1:p.Gln150=
XM_011509645.1:c.448_449delinsCA (ADAMTSL4)	XP_011507947.1:p.Gln150=
XM_011509646.1:c.349_350delinsCA (ADAMTSL4)	XP_011507948.1:p.Gln117=
XM_011509647.1:c.349_350delinsCA (ADAMTSL4)	XP_011507949.1:p.Gln117=
XM_011509648.1:c.349_350delinsCA (ADAMTSL4)	XP_011507950.1:p.Gln117=
XM_011509649.1:c.448_449delinsCA (ADAMTSL4)	XP_011507951.1:p.Gln150=
XM_011509650.1:c.448_449delinsCA (ADAMTSL4)	XP_011507952.1:p.Gln150=
XR_921844.1:n.633_634delinsCA (ADAMTSL4)
XR_922132.1:n.370+1366_370+1367delinsTG (ADAMTSL4-AS2)
XR_922133.1:n.417+1366_417+1367delinsTG (ADAMTSL4-AS2)
XM_011509644.3:c.448_449delinsCA (ADAMTSL4)	XP_011507946.1:p.Gln150=
XM_011509645.3:c.448_449delinsCA (ADAMTSL4)	XP_011507947.1:p.Gln150=
XM_011509648.3:c.349_350delinsCA (ADAMTSL4)	XP_011507950.1:p.Gln117=
XM_011509649.3:c.448_449delinsCA (ADAMTSL4)	XP_011507951.1:p.Gln150=
XM_011509650.3:c.448_449delinsCA (ADAMTSL4)	XP_011507952.1:p.Gln150=
XM_017001506.2:c.349_350delinsCA (ADAMTSL4)	XP_016856995.1:p.Gln117=
XR_001737242.2:n.606_607delinsCA (ADAMTSL4)
XR_001738226.1:n.467-244_467-243delinsTG (ADAMTSL4-AS2)
XR_001738227.1:n.466+1366_466+1367delinsTG (ADAMTSL4-AS2)
XR_001738228.1:n.372-244_372-243delinsTG (ADAMTSL4-AS2)
XR_001738229.1:n.357+2785_357+2786delinsTG (ADAMTSL4-AS2)
XR_921844.3:n.606_607delinsCA (ADAMTSL4)
NM_001288607.2:c.349_350delinsCA (ADAMTSL4)	NP_001275536.1:p.Gln117=
NM_025008.5:c.349_350delinsCA (ADAMTSL4)	NP_079284.2:p.Gln117=
NM_001288608.2:c.349_350delinsCA (ADAMTSL4)	NP_001275537.1:p.Gln117=
NM_001378596.1:c.349_350delinsCA (ADAMTSL4)	NP_001365525.1:p.Gln117=
NM_019032.6:c.349_350delinsCA (ADAMTSL4) MANE Select	NP_061905.2:p.Gln117=