Canonical Allele Identifier: CA2543494263

Gene: ADAMTSL4 ADAMTSL4-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150556827_150556828insTG , CM000663.2:g.150556827_150556828insTG	GRCh38
NC_000001.10:g.150529303_150529304insTG , CM000663.1:g.150529303_150529304insTG	GRCh37
NC_000001.9:g.148795927_148795928insTG	NCBI36
NG_012172.1:g.12406_12407insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1749+34_1749+35insTG (ADAMTSL4) MANE Select	ENSP00000271643.4:n.1749+34_1749+35insTG
ENST00000674043.1:c.1818+34_1818+35insTG (ADAMTSL4)	ENSP00000501295.1:n.1818+34_1818+35insTG
ENST00000674058.1:c.1818+34_1818+35insTG (ADAMTSL4)	ENSP00000501255.1:n.1818+34_1818+35insTG
ENST00000271643.8:c.1749+34_1749+35insTG (ADAMTSL4)	ENSP00000271643.4:n.1749+34_1749+35insTG
ENST00000369038.6:c.1749+34_1749+35insTG (ADAMTSL4)	ENSP00000358034.2:n.1749+34_1749+35insTG
ENST00000369039.9:c.1818+34_1818+35insTG (ADAMTSL4)	ENSP00000358035.5:n.1818+34_1818+35insTG
ENST00000369041.9:c.1749+34_1749+35insTG (ADAMTSL4)	ENSP00000358037.5:n.1749+34_1749+35insTG
ENST00000622417.4:c.363+34_363+35insTG (ADAMTSL4)	ENSP00000477897.1:n.363+34_363+35insTG
NM_001288607.1:c.1818+34_1818+35insTG (ADAMTSL4)	NP_001275536.1:n.1818+34_1818+35insTG
NM_001288608.1:c.1818+34_1818+35insTG (ADAMTSL4)	NP_001275537.1:n.1818+34_1818+35insTG
NM_019032.5:c.1749+34_1749+35insTG (ADAMTSL4)	NP_061905.2:n.1749+34_1749+35insTG
NM_025008.4:c.1749+34_1749+35insTG (ADAMTSL4)	NP_079284.2:n.1749+34_1749+35insTG
XM_011509644.1:c.1917+34_1917+35insTG (ADAMTSL4)	XP_011507946.1:n.1917+34_1917+35insTG
XM_011509645.1:c.1848+34_1848+35insTG (ADAMTSL4)	XP_011507947.1:n.1848+34_1848+35insTG
XM_011509646.1:c.1818+34_1818+35insTG (ADAMTSL4)	XP_011507948.1:n.1818+34_1818+35insTG
XM_011509647.1:c.1818+34_1818+35insTG (ADAMTSL4)	XP_011507949.1:n.1818+34_1818+35insTG
XM_011509648.1:c.1818+34_1818+35insTG (ADAMTSL4)	XP_011507950.1:n.1818+34_1818+35insTG
XM_011509649.1:c.1917+34_1917+35insTG (ADAMTSL4)	XP_011507951.1:n.1917+34_1917+35insTG
XM_011509650.1:c.1917+34_1917+35insTG (ADAMTSL4)	XP_011507952.1:n.1917+34_1917+35insTG
XM_011509651.1:c.426+34_426+35insTG (ADAMTSL4)	XP_011507953.1:n.426+34_426+35insTG
XM_011509652.1:c.426+34_426+35insTG (ADAMTSL4)	XP_011507954.1:n.426+34_426+35insTG
XR_921844.1:n.2102+34_2102+35insTG (ADAMTSL4)
XR_922133.1:n.140-610_140-609insAC (ADAMTSL4-AS2)
XM_011509644.3:c.1917+34_1917+35insTG (ADAMTSL4)	XP_011507946.1:n.1917+34_1917+35insTG
XM_011509645.3:c.1848+34_1848+35insTG (ADAMTSL4)	XP_011507947.1:n.1848+34_1848+35insTG
XM_011509648.3:c.1818+34_1818+35insTG (ADAMTSL4)	XP_011507950.1:n.1818+34_1818+35insTG
XM_011509649.3:c.1917+34_1917+35insTG (ADAMTSL4)	XP_011507951.1:n.1917+34_1917+35insTG
XM_011509650.3:c.1917+34_1917+35insTG (ADAMTSL4)	XP_011507952.1:n.1917+34_1917+35insTG
XM_011509651.2:c.426+34_426+35insTG (ADAMTSL4)	XP_011507953.1:n.426+34_426+35insTG
XM_011509652.2:c.426+34_426+35insTG (ADAMTSL4)	XP_011507954.1:n.426+34_426+35insTG
XM_017001506.2:c.1818+34_1818+35insTG (ADAMTSL4)	XP_016856995.1:n.1818+34_1818+35insTG
XM_017001507.1:c.163-112_163-111insTG (ADAMTSL4)	XP_016856996.1:n.163-112_163-111insTG
XR_001737242.2:n.1903-112_1903-111insTG (ADAMTSL4)
XR_921844.3:n.2075+34_2075+35insTG (ADAMTSL4)
NM_001288607.2:c.1818+34_1818+35insTG (ADAMTSL4)	NP_001275536.1:n.1818+34_1818+35insTG
NM_025008.5:c.1749+34_1749+35insTG (ADAMTSL4)	NP_079284.2:n.1749+34_1749+35insTG
NM_001288608.2:c.1818+34_1818+35insTG (ADAMTSL4)	NP_001275537.1:n.1818+34_1818+35insTG
NM_001378596.1:c.1749+34_1749+35insTG (ADAMTSL4)	NP_001365525.1:n.1749+34_1749+35insTG
NM_019032.6:c.1749+34_1749+35insTG (ADAMTSL4) MANE Select	NP_061905.2:n.1749+34_1749+35insTG