Canonical Allele Identifier: CA526260762

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• dbSNP Id: rs1351102431
• gnomAD v2: 1-150525871-C-CTG
• MyVariant Identifiers: chr1:g.150525871_150525872insTG (hg19) ; chr1:g.150553395_150553396insTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150553398_150553399dup , CM000663.2:g.150553398_150553399dup	GRCh38
NC_000001.10:g.150525874_150525875dup , CM000663.1:g.150525874_150525875dup	GRCh37
NC_000001.9:g.148792498_148792499dup	NCBI36
NG_012172.1:g.8977_8978dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.435-28_435-27dup (ADAMTSL4) MANE Select	ENSP00000271643.4:n.435-28_435-27dup
ENST00000674043.1:c.435-28_435-27dup (ADAMTSL4)	ENSP00000501295.1:n.435-28_435-27dup
ENST00000674058.1:c.435-28_435-27dup (ADAMTSL4)	ENSP00000501255.1:n.435-28_435-27dup
ENST00000271643.8:c.435-28_435-27dup (ADAMTSL4)	ENSP00000271643.4:n.435-28_435-27dup
ENST00000369038.6:c.435-28_435-27dup (ADAMTSL4)	ENSP00000358034.2:n.435-28_435-27dup
ENST00000369039.9:c.435-28_435-27dup (ADAMTSL4)	ENSP00000358035.5:n.435-28_435-27dup
ENST00000369041.9:c.435-28_435-27dup (ADAMTSL4)	ENSP00000358037.5:n.435-28_435-27dup
NM_001288607.1:c.435-28_435-27dup (ADAMTSL4)	NP_001275536.1:n.435-28_435-27dup
NM_001288608.1:c.435-28_435-27dup (ADAMTSL4)	NP_001275537.1:n.435-28_435-27dup
NM_019032.5:c.435-28_435-27dup (ADAMTSL4)	NP_061905.2:n.435-28_435-27dup
NM_025008.4:c.435-28_435-27dup (ADAMTSL4)	NP_079284.2:n.435-28_435-27dup
XM_011509644.1:c.534-28_534-27dup (ADAMTSL4)	XP_011507946.1:n.534-28_534-27dup
XM_011509645.1:c.534-28_534-27dup (ADAMTSL4)	XP_011507947.1:n.534-28_534-27dup
XM_011509646.1:c.435-28_435-27dup (ADAMTSL4)	XP_011507948.1:n.435-28_435-27dup
XM_011509647.1:c.435-28_435-27dup (ADAMTSL4)	XP_011507949.1:n.435-28_435-27dup
XM_011509648.1:c.435-28_435-27dup (ADAMTSL4)	XP_011507950.1:n.435-28_435-27dup
XM_011509649.1:c.534-28_534-27dup (ADAMTSL4)	XP_011507951.1:n.534-28_534-27dup
XM_011509650.1:c.534-28_534-27dup (ADAMTSL4)	XP_011507952.1:n.534-28_534-27dup
XR_921844.1:n.719-28_719-27dup (ADAMTSL4)
XR_922132.1:n.370+1138_370+1139dup (ADAMTSL4-AS2)
XR_922133.1:n.417+1138_417+1139dup (ADAMTSL4-AS2)
XM_011509644.3:c.534-28_534-27dup (ADAMTSL4)	XP_011507946.1:n.534-28_534-27dup
XM_011509645.3:c.534-28_534-27dup (ADAMTSL4)	XP_011507947.1:n.534-28_534-27dup
XM_011509648.3:c.435-28_435-27dup (ADAMTSL4)	XP_011507950.1:n.435-28_435-27dup
XM_011509649.3:c.534-28_534-27dup (ADAMTSL4)	XP_011507951.1:n.534-28_534-27dup
XM_011509650.3:c.534-28_534-27dup (ADAMTSL4)	XP_011507952.1:n.534-28_534-27dup
XM_017001506.2:c.435-28_435-27dup (ADAMTSL4)	XP_016856995.1:n.435-28_435-27dup
XR_001737242.2:n.692-28_692-27dup (ADAMTSL4)
XR_001738226.1:n.467-472_467-471dup (ADAMTSL4-AS2)
XR_001738227.1:n.466+1138_466+1139dup (ADAMTSL4-AS2)
XR_001738228.1:n.372-472_372-471dup (ADAMTSL4-AS2)
XR_001738229.1:n.357+2557_357+2558dup (ADAMTSL4-AS2)
XR_921844.3:n.692-28_692-27dup (ADAMTSL4)
NM_001288607.2:c.435-28_435-27dup (ADAMTSL4)	NP_001275536.1:n.435-28_435-27dup
NM_025008.5:c.435-28_435-27dup (ADAMTSL4)	NP_079284.2:n.435-28_435-27dup
NM_001288608.2:c.435-28_435-27dup (ADAMTSL4)	NP_001275537.1:n.435-28_435-27dup
NM_001378596.1:c.435-28_435-27dup (ADAMTSL4)	NP_001365525.1:n.435-28_435-27dup
NM_019032.6:c.435-28_435-27dup (ADAMTSL4) MANE Select	NP_061905.2:n.435-28_435-27dup