Canonical Allele Identifier: CA2697295123

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• dbSNP Id: rs2101634834

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150557183_150557184insCCCCCC , CM000663.2:g.150557183_150557184insCCCCCC	GRCh38
NC_000001.10:g.150529659_150529660insCCCCCC , CM000663.1:g.150529659_150529660insCCCCCC	GRCh37
NC_000001.9:g.148796283_148796284insCCCCCC	NCBI36
NG_012172.1:g.12762_12763insCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1895_1896insCCCCCC (ADAMTSL4) MANE Select	ENSP00000271643.4:p.Ala632_Pro633insProPro
ENST00000674043.1:c.1964_1965insCCCCCC (ADAMTSL4)	ENSP00000501295.1:p.Ala655_Pro656insProPro
ENST00000674058.1:c.1857-79_1857-78insCCCCCC (ADAMTSL4)	ENSP00000501255.1:n.1857-79_1857-78insCCCCCC
ENST00000271643.8:c.1895_1896insCCCCCC (ADAMTSL4)	ENSP00000271643.4:p.Ala632_Pro633insProPro
ENST00000369038.6:c.1895_1896insCCCCCC (ADAMTSL4)	ENSP00000358034.2:p.Ala632_Pro633insProPro
ENST00000369039.9:c.1964_1965insCCCCCC (ADAMTSL4)	ENSP00000358035.5:p.Ala655_Pro656insProPro
ENST00000369041.9:c.1895_1896insCCCCCC (ADAMTSL4)	ENSP00000358037.5:p.Ala632_Pro633insProPro
ENST00000622417.4:c.509_510insCCCCCC (ADAMTSL4)	ENSP00000477897.1:p.Ala170_Pro171insProPro
NM_001288607.1:c.1857-79_1857-78insCCCCCC (ADAMTSL4)	NP_001275536.1:n.1857-79_1857-78insCCCCCC
NM_001288608.1:c.1964_1965insCCCCCC (ADAMTSL4)	NP_001275537.1:p.Ala655_Pro656insProPro
NM_019032.5:c.1895_1896insCCCCCC (ADAMTSL4)	NP_061905.2:p.Ala632_Pro633insProPro
NM_025008.4:c.1895_1896insCCCCCC (ADAMTSL4)	NP_079284.2:p.Ala632_Pro633insProPro
XM_011509644.1:c.2063_2064insCCCCCC (ADAMTSL4)	XP_011507946.1:p.Ala688_Pro689insProPro
XM_011509645.1:c.1994_1995insCCCCCC (ADAMTSL4)	XP_011507947.1:p.Ala665_Pro666insProPro
XM_011509646.1:c.1964_1965insCCCCCC (ADAMTSL4)	XP_011507948.1:p.Ala655_Pro656insProPro
XM_011509647.1:c.1964_1965insCCCCCC (ADAMTSL4)	XP_011507949.1:p.Ala655_Pro656insProPro
XM_011509648.1:c.1964_1965insCCCCCC (ADAMTSL4)	XP_011507950.1:p.Ala655_Pro656insProPro
XM_011509649.1:c.2063_2064insCCCCCC (ADAMTSL4)	XP_011507951.1:p.Ala688_Pro689insProPro
XM_011509650.1:c.2063_2064insCCCCCC (ADAMTSL4)	XP_011507952.1:p.Ala688_Pro689insProPro
XM_011509651.1:c.572_573insCCCCCC (ADAMTSL4)	XP_011507953.1:p.Ala191_Pro192insProPro
XM_011509652.1:c.572_573insCCCCCC (ADAMTSL4)	XP_011507954.1:p.Ala191_Pro192insProPro
XR_921844.1:n.2248_2249insCCCCCC (ADAMTSL4)
XR_922133.1:n.139+510_139+511insGGGGGG (ADAMTSL4-AS2)
XM_011509644.3:c.2063_2064insCCCCCC (ADAMTSL4)	XP_011507946.1:p.Ala688_Pro689insProPro
XM_011509645.3:c.1994_1995insCCCCCC (ADAMTSL4)	XP_011507947.1:p.Ala665_Pro666insProPro
XM_011509648.3:c.1964_1965insCCCCCC (ADAMTSL4)	XP_011507950.1:p.Ala655_Pro656insProPro
XM_011509649.3:c.2063_2064insCCCCCC (ADAMTSL4)	XP_011507951.1:p.Ala688_Pro689insProPro
XM_011509650.3:c.2063_2064insCCCCCC (ADAMTSL4)	XP_011507952.1:p.Ala688_Pro689insProPro
XM_011509651.2:c.572_573insCCCCCC (ADAMTSL4)	XP_011507953.1:p.Ala191_Pro192insProPro
XM_011509652.2:c.572_573insCCCCCC (ADAMTSL4)	XP_011507954.1:p.Ala191_Pro192insProPro
XM_017001506.2:c.1964_1965insCCCCCC (ADAMTSL4)	XP_016856995.1:p.Ala655_Pro656insProPro
XM_017001507.1:c.308_309insCCCCCC (ADAMTSL4)	XP_016856996.1:p.Ala103_Pro104insProPro
XR_001737242.2:n.2048_2049insCCCCCC (ADAMTSL4)
XR_921844.3:n.2221_2222insCCCCCC (ADAMTSL4)
NM_001288607.2:c.1857-79_1857-78insCCCCCC (ADAMTSL4)	NP_001275536.1:n.1857-79_1857-78insCCCCCC
NM_025008.5:c.1895_1896insCCCCCC (ADAMTSL4)	NP_079284.2:p.Ala632_Pro633insProPro
NM_001288608.2:c.1964_1965insCCCCCC (ADAMTSL4)	NP_001275537.1:p.Ala655_Pro656insProPro
NM_001378596.1:c.1895_1896insCCCCCC (ADAMTSL4)	NP_001365525.1:p.Ala632_Pro633insProPro
NM_019032.6:c.1895_1896insCCCCCC (ADAMTSL4) MANE Select	NP_061905.2:p.Ala632_Pro633insProPro