Canonical Allele Identifier: CA2479210760

Gene: ADAMTSL4 ADAMTSL4-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150557061_150557062delinsGA , CM000663.2:g.150557061_150557062delinsGA	GRCh38
NC_000001.10:g.150529537_150529538delinsGA , CM000663.1:g.150529537_150529538delinsGA	GRCh37
NC_000001.9:g.148796161_148796162delinsGA	NCBI36
NG_012172.1:g.12640_12641delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1861+11_1861+12delinsGA (ADAMTSL4) MANE Select	ENSP00000271643.4:n.1861+11_1861+12delinsGA
ENST00000674043.1:c.1930+11_1930+12delinsGA (ADAMTSL4)	ENSP00000501295.1:n.1930+11_1930+12delinsGA
ENST00000674058.1:c.1856+85_1856+86delinsGA (ADAMTSL4)	ENSP00000501255.1:n.1856+85_1856+86delinsGA
ENST00000271643.8:c.1861+11_1861+12delinsGA (ADAMTSL4)	ENSP00000271643.4:n.1861+11_1861+12delinsGA
ENST00000369038.6:c.1861+11_1861+12delinsGA (ADAMTSL4)	ENSP00000358034.2:n.1861+11_1861+12delinsGA
ENST00000369039.9:c.1930+11_1930+12delinsGA (ADAMTSL4)	ENSP00000358035.5:n.1930+11_1930+12delinsGA
ENST00000369041.9:c.1861+11_1861+12delinsGA (ADAMTSL4)	ENSP00000358037.5:n.1861+11_1861+12delinsGA
ENST00000622417.4:c.475+11_475+12delinsGA (ADAMTSL4)	ENSP00000477897.1:n.475+11_475+12delinsGA
NM_001288607.1:c.1856+85_1856+86delinsGA (ADAMTSL4)	NP_001275536.1:n.1856+85_1856+86delinsGA
NM_001288608.1:c.1930+11_1930+12delinsGA (ADAMTSL4)	NP_001275537.1:n.1930+11_1930+12delinsGA
NM_019032.5:c.1861+11_1861+12delinsGA (ADAMTSL4)	NP_061905.2:n.1861+11_1861+12delinsGA
NM_025008.4:c.1861+11_1861+12delinsGA (ADAMTSL4)	NP_079284.2:n.1861+11_1861+12delinsGA
XM_011509644.1:c.2029+11_2029+12delinsGA (ADAMTSL4)	XP_011507946.1:n.2029+11_2029+12delinsGA
XM_011509645.1:c.1960+11_1960+12delinsGA (ADAMTSL4)	XP_011507947.1:n.1960+11_1960+12delinsGA
XM_011509646.1:c.1930+11_1930+12delinsGA (ADAMTSL4)	XP_011507948.1:n.1930+11_1930+12delinsGA
XM_011509647.1:c.1930+11_1930+12delinsGA (ADAMTSL4)	XP_011507949.1:n.1930+11_1930+12delinsGA
XM_011509648.1:c.1930+11_1930+12delinsGA (ADAMTSL4)	XP_011507950.1:n.1930+11_1930+12delinsGA
XM_011509649.1:c.2029+11_2029+12delinsGA (ADAMTSL4)	XP_011507951.1:n.2029+11_2029+12delinsGA
XM_011509650.1:c.2029+11_2029+12delinsGA (ADAMTSL4)	XP_011507952.1:n.2029+11_2029+12delinsGA
XM_011509651.1:c.538+11_538+12delinsGA (ADAMTSL4)	XP_011507953.1:n.538+11_538+12delinsGA
XM_011509652.1:c.538+11_538+12delinsGA (ADAMTSL4)	XP_011507954.1:n.538+11_538+12delinsGA
XR_921844.1:n.2214+11_2214+12delinsGA (ADAMTSL4)
XR_922133.1:n.139+631_139+632delinsTC (ADAMTSL4-AS2)
XM_011509644.3:c.2029+11_2029+12delinsGA (ADAMTSL4)	XP_011507946.1:n.2029+11_2029+12delinsGA
XM_011509645.3:c.1960+11_1960+12delinsGA (ADAMTSL4)	XP_011507947.1:n.1960+11_1960+12delinsGA
XM_011509648.3:c.1930+11_1930+12delinsGA (ADAMTSL4)	XP_011507950.1:n.1930+11_1930+12delinsGA
XM_011509649.3:c.2029+11_2029+12delinsGA (ADAMTSL4)	XP_011507951.1:n.2029+11_2029+12delinsGA
XM_011509650.3:c.2029+11_2029+12delinsGA (ADAMTSL4)	XP_011507952.1:n.2029+11_2029+12delinsGA
XM_011509651.2:c.538+11_538+12delinsGA (ADAMTSL4)	XP_011507953.1:n.538+11_538+12delinsGA
XM_011509652.2:c.538+11_538+12delinsGA (ADAMTSL4)	XP_011507954.1:n.538+11_538+12delinsGA
XM_017001506.2:c.1930+11_1930+12delinsGA (ADAMTSL4)	XP_016856995.1:n.1930+11_1930+12delinsGA
XM_017001507.1:c.274+11_274+12delinsGA (ADAMTSL4)	XP_016856996.1:n.274+11_274+12delinsGA
XR_001737242.2:n.2014+11_2014+12delinsGA (ADAMTSL4)
XR_921844.3:n.2187+11_2187+12delinsGA (ADAMTSL4)
NM_001288607.2:c.1856+85_1856+86delinsGA (ADAMTSL4)	NP_001275536.1:n.1856+85_1856+86delinsGA
NM_025008.5:c.1861+11_1861+12delinsGA (ADAMTSL4)	NP_079284.2:n.1861+11_1861+12delinsGA
NM_001288608.2:c.1930+11_1930+12delinsGA (ADAMTSL4)	NP_001275537.1:n.1930+11_1930+12delinsGA
NM_001378596.1:c.1861+11_1861+12delinsGA (ADAMTSL4)	NP_001365525.1:n.1861+11_1861+12delinsGA
NM_019032.6:c.1861+11_1861+12delinsGA (ADAMTSL4) MANE Select	NP_061905.2:n.1861+11_1861+12delinsGA