Canonical Allele Identifier: CA342313339

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• MyVariant Identifiers: chr1:g.150529462C>G (hg19) ; chr1:g.150556986C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150556986C>G , CM000663.2:g.150556986C>G	GRCh38
NC_000001.10:g.150529462C>G , CM000663.1:g.150529462C>G	GRCh37
NC_000001.9:g.148796086C>G	NCBI36
NG_012172.1:g.12565C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000271643.9:c.1797C>G (ADAMTSL4) MANE Select	ENSP00000271643.4:p.Ile599Met
ENST00000674043.1:c.1866C>G (ADAMTSL4)	ENSP00000501295.1:p.Ile622Met
ENST00000674058.1:c.1856+10C>G (ADAMTSL4)	ENSP00000501255.1:n.1856+10C>G
ENST00000271643.8:c.1797C>G (ADAMTSL4)	ENSP00000271643.4:p.Ile599Met
ENST00000369038.6:c.1797C>G (ADAMTSL4)	ENSP00000358034.2:p.Ile599Met
ENST00000369039.9:c.1866C>G (ADAMTSL4)	ENSP00000358035.5:p.Ile622Met
ENST00000369041.9:c.1797C>G (ADAMTSL4)	ENSP00000358037.5:p.Ile599Met
ENST00000622417.4:c.411C>G (ADAMTSL4)	ENSP00000477897.1:p.Ile137Met
NM_001288607.1:c.1856+10C>G (ADAMTSL4)	NP_001275536.1:n.1856+10C>G
NM_001288608.1:c.1866C>G (ADAMTSL4)	NP_001275537.1:p.Ile622Met
NM_019032.5:c.1797C>G (ADAMTSL4)	NP_061905.2:p.Ile599Met
NM_025008.4:c.1797C>G (ADAMTSL4)	NP_079284.2:p.Ile599Met
XM_011509644.1:c.1965C>G (ADAMTSL4)	XP_011507946.1:p.Ile655Met
XM_011509645.1:c.1896C>G (ADAMTSL4)	XP_011507947.1:p.Ile632Met
XM_011509646.1:c.1866C>G (ADAMTSL4)	XP_011507948.1:p.Ile622Met
XM_011509647.1:c.1866C>G (ADAMTSL4)	XP_011507949.1:p.Ile622Met
XM_011509648.1:c.1866C>G (ADAMTSL4)	XP_011507950.1:p.Ile622Met
XM_011509649.1:c.1965C>G (ADAMTSL4)	XP_011507951.1:p.Ile655Met
XM_011509650.1:c.1965C>G (ADAMTSL4)	XP_011507952.1:p.Ile655Met
XM_011509651.1:c.474C>G (ADAMTSL4)	XP_011507953.1:p.Ile158Met
XM_011509652.1:c.474C>G (ADAMTSL4)	XP_011507954.1:p.Ile158Met
XR_921844.1:n.2150C>G (ADAMTSL4)
XR_922133.1:n.139+707G>C (ADAMTSL4-AS2)
XM_011509644.3:c.1965C>G (ADAMTSL4)	XP_011507946.1:p.Ile655Met
XM_011509645.3:c.1896C>G (ADAMTSL4)	XP_011507947.1:p.Ile632Met
XM_011509648.3:c.1866C>G (ADAMTSL4)	XP_011507950.1:p.Ile622Met
XM_011509649.3:c.1965C>G (ADAMTSL4)	XP_011507951.1:p.Ile655Met
XM_011509650.3:c.1965C>G (ADAMTSL4)	XP_011507952.1:p.Ile655Met
XM_011509651.2:c.474C>G (ADAMTSL4)	XP_011507953.1:p.Ile158Met
XM_011509652.2:c.474C>G (ADAMTSL4)	XP_011507954.1:p.Ile158Met
XM_017001506.2:c.1866C>G (ADAMTSL4)	XP_016856995.1:p.Ile622Met
XM_017001507.1:c.210C>G (ADAMTSL4)	XP_016856996.1:p.Ile70Met
XR_001737242.2:n.1950C>G (ADAMTSL4)
XR_921844.3:n.2123C>G (ADAMTSL4)
NM_001288607.2:c.1856+10C>G (ADAMTSL4)	NP_001275536.1:n.1856+10C>G
NM_025008.5:c.1797C>G (ADAMTSL4)	NP_079284.2:p.Ile599Met
NM_001288608.2:c.1866C>G (ADAMTSL4)	NP_001275537.1:p.Ile622Met
NM_001378596.1:c.1797C>G (ADAMTSL4)	NP_001365525.1:p.Ile599Met
NM_019032.6:c.1797C>G (ADAMTSL4) MANE Select	NP_061905.2:p.Ile599Met