Canonical Allele Identifier: CA2647815604

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• gnomAD v4: 1-150556913-TATTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150556917_150556920del , CM000663.2:g.150556917_150556920del	GRCh38
NC_000001.10:g.150529393_150529396del , CM000663.1:g.150529393_150529396del	GRCh37
NC_000001.9:g.148796017_148796020del	NCBI36
NG_012172.1:g.12496_12499del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1750-22_1750-19del (ADAMTSL4) MANE Select	ENSP00000271643.4:n.1750-22_1750-19del
ENST00000674043.1:c.1819-22_1819-19del (ADAMTSL4)	ENSP00000501295.1:n.1819-22_1819-19del
ENST00000674058.1:c.1819-22_1819-19del (ADAMTSL4)	ENSP00000501255.1:n.1819-22_1819-19del
ENST00000271643.8:c.1750-22_1750-19del (ADAMTSL4)	ENSP00000271643.4:n.1750-22_1750-19del
ENST00000369038.6:c.1750-22_1750-19del (ADAMTSL4)	ENSP00000358034.2:n.1750-22_1750-19del
ENST00000369039.9:c.1819-22_1819-19del (ADAMTSL4)	ENSP00000358035.5:n.1819-22_1819-19del
ENST00000369041.9:c.1750-22_1750-19del (ADAMTSL4)	ENSP00000358037.5:n.1750-22_1750-19del
ENST00000622417.4:c.364-22_364-19del (ADAMTSL4)	ENSP00000477897.1:n.364-22_364-19del
NM_001288607.1:c.1819-22_1819-19del (ADAMTSL4)	NP_001275536.1:n.1819-22_1819-19del
NM_001288608.1:c.1819-22_1819-19del (ADAMTSL4)	NP_001275537.1:n.1819-22_1819-19del
NM_019032.5:c.1750-22_1750-19del (ADAMTSL4)	NP_061905.2:n.1750-22_1750-19del
NM_025008.4:c.1750-22_1750-19del (ADAMTSL4)	NP_079284.2:n.1750-22_1750-19del
XM_011509644.1:c.1918-22_1918-19del (ADAMTSL4)	XP_011507946.1:n.1918-22_1918-19del
XM_011509645.1:c.1849-22_1849-19del (ADAMTSL4)	XP_011507947.1:n.1849-22_1849-19del
XM_011509646.1:c.1819-22_1819-19del (ADAMTSL4)	XP_011507948.1:n.1819-22_1819-19del
XM_011509647.1:c.1819-22_1819-19del (ADAMTSL4)	XP_011507949.1:n.1819-22_1819-19del
XM_011509648.1:c.1819-22_1819-19del (ADAMTSL4)	XP_011507950.1:n.1819-22_1819-19del
XM_011509649.1:c.1918-22_1918-19del (ADAMTSL4)	XP_011507951.1:n.1918-22_1918-19del
XM_011509650.1:c.1918-22_1918-19del (ADAMTSL4)	XP_011507952.1:n.1918-22_1918-19del
XM_011509651.1:c.427-22_427-19del (ADAMTSL4)	XP_011507953.1:n.427-22_427-19del
XM_011509652.1:c.427-22_427-19del (ADAMTSL4)	XP_011507954.1:n.427-22_427-19del
XR_921844.1:n.2103-22_2103-19del (ADAMTSL4)
XR_922133.1:n.140-700_140-697del (ADAMTSL4-AS2)
XM_011509644.3:c.1918-22_1918-19del (ADAMTSL4)	XP_011507946.1:n.1918-22_1918-19del
XM_011509645.3:c.1849-22_1849-19del (ADAMTSL4)	XP_011507947.1:n.1849-22_1849-19del
XM_011509648.3:c.1819-22_1819-19del (ADAMTSL4)	XP_011507950.1:n.1819-22_1819-19del
XM_011509649.3:c.1918-22_1918-19del (ADAMTSL4)	XP_011507951.1:n.1918-22_1918-19del
XM_011509650.3:c.1918-22_1918-19del (ADAMTSL4)	XP_011507952.1:n.1918-22_1918-19del
XM_011509651.2:c.427-22_427-19del (ADAMTSL4)	XP_011507953.1:n.427-22_427-19del
XM_011509652.2:c.427-22_427-19del (ADAMTSL4)	XP_011507954.1:n.427-22_427-19del
XM_017001506.2:c.1819-22_1819-19del (ADAMTSL4)	XP_016856995.1:n.1819-22_1819-19del
XM_017001507.1:c.163-22_163-19del (ADAMTSL4)	XP_016856996.1:n.163-22_163-19del
XR_001737242.2:n.1903-22_1903-19del (ADAMTSL4)
XR_921844.3:n.2076-22_2076-19del (ADAMTSL4)
NM_001288607.2:c.1819-22_1819-19del (ADAMTSL4)	NP_001275536.1:n.1819-22_1819-19del
NM_025008.5:c.1750-22_1750-19del (ADAMTSL4)	NP_079284.2:n.1750-22_1750-19del
NM_001288608.2:c.1819-22_1819-19del (ADAMTSL4)	NP_001275537.1:n.1819-22_1819-19del
NM_001378596.1:c.1750-22_1750-19del (ADAMTSL4)	NP_001365525.1:n.1750-22_1750-19del
NM_019032.6:c.1750-22_1750-19del (ADAMTSL4) MANE Select	NP_061905.2:n.1750-22_1750-19del