Canonical Allele Identifier: CA342313174

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• MyVariant Identifiers: chr1:g.150529417G>C (hg19) ; chr1:g.150556941G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150556941G>C , CM000663.2:g.150556941G>C	GRCh38
NC_000001.10:g.150529417G>C , CM000663.1:g.150529417G>C	GRCh37
NC_000001.9:g.148796041G>C	NCBI36
NG_012172.1:g.12520G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1752G>C (ADAMTSL4) MANE Select	ENSP00000271643.4:p.Met584Ile
ENST00000674043.1:c.1821G>C (ADAMTSL4)	ENSP00000501295.1:p.Met607Ile
ENST00000674058.1:c.1821G>C (ADAMTSL4)	ENSP00000501255.1:p.Met607Ile
ENST00000271643.8:c.1752G>C (ADAMTSL4)	ENSP00000271643.4:p.Met584Ile
ENST00000369038.6:c.1752G>C (ADAMTSL4)	ENSP00000358034.2:p.Met584Ile
ENST00000369039.9:c.1821G>C (ADAMTSL4)	ENSP00000358035.5:p.Met607Ile
ENST00000369041.9:c.1752G>C (ADAMTSL4)	ENSP00000358037.5:p.Met584Ile
ENST00000622417.4:c.366G>C (ADAMTSL4)	ENSP00000477897.1:p.Met122Ile
NM_001288607.1:c.1821G>C (ADAMTSL4)	NP_001275536.1:p.Met607Ile
NM_001288608.1:c.1821G>C (ADAMTSL4)	NP_001275537.1:p.Met607Ile
NM_019032.5:c.1752G>C (ADAMTSL4)	NP_061905.2:p.Met584Ile
NM_025008.4:c.1752G>C (ADAMTSL4)	NP_079284.2:p.Met584Ile
XM_011509644.1:c.1920G>C (ADAMTSL4)	XP_011507946.1:p.Met640Ile
XM_011509645.1:c.1851G>C (ADAMTSL4)	XP_011507947.1:p.Met617Ile
XM_011509646.1:c.1821G>C (ADAMTSL4)	XP_011507948.1:p.Met607Ile
XM_011509647.1:c.1821G>C (ADAMTSL4)	XP_011507949.1:p.Met607Ile
XM_011509648.1:c.1821G>C (ADAMTSL4)	XP_011507950.1:p.Met607Ile
XM_011509649.1:c.1920G>C (ADAMTSL4)	XP_011507951.1:p.Met640Ile
XM_011509650.1:c.1920G>C (ADAMTSL4)	XP_011507952.1:p.Met640Ile
XM_011509651.1:c.429G>C (ADAMTSL4)	XP_011507953.1:p.Met143Ile
XM_011509652.1:c.429G>C (ADAMTSL4)	XP_011507954.1:p.Met143Ile
XR_921844.1:n.2105G>C (ADAMTSL4)
XR_922133.1:n.140-724C>G (ADAMTSL4-AS2)
XM_011509644.3:c.1920G>C (ADAMTSL4)	XP_011507946.1:p.Met640Ile
XM_011509645.3:c.1851G>C (ADAMTSL4)	XP_011507947.1:p.Met617Ile
XM_011509648.3:c.1821G>C (ADAMTSL4)	XP_011507950.1:p.Met607Ile
XM_011509649.3:c.1920G>C (ADAMTSL4)	XP_011507951.1:p.Met640Ile
XM_011509650.3:c.1920G>C (ADAMTSL4)	XP_011507952.1:p.Met640Ile
XM_011509651.2:c.429G>C (ADAMTSL4)	XP_011507953.1:p.Met143Ile
XM_011509652.2:c.429G>C (ADAMTSL4)	XP_011507954.1:p.Met143Ile
XM_017001506.2:c.1821G>C (ADAMTSL4)	XP_016856995.1:p.Met607Ile
XM_017001507.1:c.165G>C (ADAMTSL4)	XP_016856996.1:p.Met55Ile
XR_001737242.2:n.1905G>C (ADAMTSL4)
XR_921844.3:n.2078G>C (ADAMTSL4)
NM_001288607.2:c.1821G>C (ADAMTSL4)	NP_001275536.1:p.Met607Ile
NM_025008.5:c.1752G>C (ADAMTSL4)	NP_079284.2:p.Met584Ile
NM_001288608.2:c.1821G>C (ADAMTSL4)	NP_001275537.1:p.Met607Ile
NM_001378596.1:c.1752G>C (ADAMTSL4)	NP_001365525.1:p.Met584Ile
NM_019032.6:c.1752G>C (ADAMTSL4) MANE Select	NP_061905.2:p.Met584Ile