Canonical Allele Identifier: CA2647815565

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• gnomAD v4: 1-150556831-G-GGA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150556833_150556834dup , CM000663.2:g.150556833_150556834dup	GRCh38
NC_000001.10:g.150529309_150529310dup , CM000663.1:g.150529309_150529310dup	GRCh37
NC_000001.9:g.148795933_148795934dup	NCBI36
NG_012172.1:g.12412_12413dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1749+40_1749+41dup (ADAMTSL4) MANE Select	ENSP00000271643.4:n.1749+40_1749+41dup
ENST00000674043.1:c.1818+40_1818+41dup (ADAMTSL4)	ENSP00000501295.1:n.1818+40_1818+41dup
ENST00000674058.1:c.1818+40_1818+41dup (ADAMTSL4)	ENSP00000501255.1:n.1818+40_1818+41dup
ENST00000271643.8:c.1749+40_1749+41dup (ADAMTSL4)	ENSP00000271643.4:n.1749+40_1749+41dup
ENST00000369038.6:c.1749+40_1749+41dup (ADAMTSL4)	ENSP00000358034.2:n.1749+40_1749+41dup
ENST00000369039.9:c.1818+40_1818+41dup (ADAMTSL4)	ENSP00000358035.5:n.1818+40_1818+41dup
ENST00000369041.9:c.1749+40_1749+41dup (ADAMTSL4)	ENSP00000358037.5:n.1749+40_1749+41dup
ENST00000622417.4:c.363+40_363+41dup (ADAMTSL4)	ENSP00000477897.1:n.363+40_363+41dup
NM_001288607.1:c.1818+40_1818+41dup (ADAMTSL4)	NP_001275536.1:n.1818+40_1818+41dup
NM_001288608.1:c.1818+40_1818+41dup (ADAMTSL4)	NP_001275537.1:n.1818+40_1818+41dup
NM_019032.5:c.1749+40_1749+41dup (ADAMTSL4)	NP_061905.2:n.1749+40_1749+41dup
NM_025008.4:c.1749+40_1749+41dup (ADAMTSL4)	NP_079284.2:n.1749+40_1749+41dup
XM_011509644.1:c.1917+40_1917+41dup (ADAMTSL4)	XP_011507946.1:n.1917+40_1917+41dup
XM_011509645.1:c.1848+40_1848+41dup (ADAMTSL4)	XP_011507947.1:n.1848+40_1848+41dup
XM_011509646.1:c.1818+40_1818+41dup (ADAMTSL4)	XP_011507948.1:n.1818+40_1818+41dup
XM_011509647.1:c.1818+40_1818+41dup (ADAMTSL4)	XP_011507949.1:n.1818+40_1818+41dup
XM_011509648.1:c.1818+40_1818+41dup (ADAMTSL4)	XP_011507950.1:n.1818+40_1818+41dup
XM_011509649.1:c.1917+40_1917+41dup (ADAMTSL4)	XP_011507951.1:n.1917+40_1917+41dup
XM_011509650.1:c.1917+40_1917+41dup (ADAMTSL4)	XP_011507952.1:n.1917+40_1917+41dup
XM_011509651.1:c.426+40_426+41dup (ADAMTSL4)	XP_011507953.1:n.426+40_426+41dup
XM_011509652.1:c.426+40_426+41dup (ADAMTSL4)	XP_011507954.1:n.426+40_426+41dup
XR_921844.1:n.2102+40_2102+41dup (ADAMTSL4)
XR_922133.1:n.140-616_140-615dup (ADAMTSL4-AS2)
XM_011509644.3:c.1917+40_1917+41dup (ADAMTSL4)	XP_011507946.1:n.1917+40_1917+41dup
XM_011509645.3:c.1848+40_1848+41dup (ADAMTSL4)	XP_011507947.1:n.1848+40_1848+41dup
XM_011509648.3:c.1818+40_1818+41dup (ADAMTSL4)	XP_011507950.1:n.1818+40_1818+41dup
XM_011509649.3:c.1917+40_1917+41dup (ADAMTSL4)	XP_011507951.1:n.1917+40_1917+41dup
XM_011509650.3:c.1917+40_1917+41dup (ADAMTSL4)	XP_011507952.1:n.1917+40_1917+41dup
XM_011509651.2:c.426+40_426+41dup (ADAMTSL4)	XP_011507953.1:n.426+40_426+41dup
XM_011509652.2:c.426+40_426+41dup (ADAMTSL4)	XP_011507954.1:n.426+40_426+41dup
XM_017001506.2:c.1818+40_1818+41dup (ADAMTSL4)	XP_016856995.1:n.1818+40_1818+41dup
XM_017001507.1:c.163-106_163-105dup (ADAMTSL4)	XP_016856996.1:n.163-106_163-105dup
XR_001737242.2:n.1903-106_1903-105dup (ADAMTSL4)
XR_921844.3:n.2075+40_2075+41dup (ADAMTSL4)
NM_001288607.2:c.1818+40_1818+41dup (ADAMTSL4)	NP_001275536.1:n.1818+40_1818+41dup
NM_025008.5:c.1749+40_1749+41dup (ADAMTSL4)	NP_079284.2:n.1749+40_1749+41dup
NM_001288608.2:c.1818+40_1818+41dup (ADAMTSL4)	NP_001275537.1:n.1818+40_1818+41dup
NM_001378596.1:c.1749+40_1749+41dup (ADAMTSL4)	NP_001365525.1:n.1749+40_1749+41dup
NM_019032.6:c.1749+40_1749+41dup (ADAMTSL4) MANE Select	NP_061905.2:n.1749+40_1749+41dup