Canonical Allele Identifier: CA342313417

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• MyVariant Identifiers: chr1:g.150529501G>T (hg19) ; chr1:g.150557025G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150557025G>T , CM000663.2:g.150557025G>T	GRCh38
NC_000001.10:g.150529501G>T , CM000663.1:g.150529501G>T	GRCh37
NC_000001.9:g.148796125G>T	NCBI36
NG_012172.1:g.12604G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1836G>T (ADAMTSL4) MANE Select	ENSP00000271643.4:p.Glu612Asp
ENST00000674043.1:c.1905G>T (ADAMTSL4)	ENSP00000501295.1:p.Glu635Asp
ENST00000674058.1:c.1856+49G>T (ADAMTSL4)	ENSP00000501255.1:n.1856+49G>T
ENST00000271643.8:c.1836G>T (ADAMTSL4)	ENSP00000271643.4:p.Glu612Asp
ENST00000369038.6:c.1836G>T (ADAMTSL4)	ENSP00000358034.2:p.Glu612Asp
ENST00000369039.9:c.1905G>T (ADAMTSL4)	ENSP00000358035.5:p.Glu635Asp
ENST00000369041.9:c.1836G>T (ADAMTSL4)	ENSP00000358037.5:p.Glu612Asp
ENST00000622417.4:c.450G>T (ADAMTSL4)	ENSP00000477897.1:p.Glu150Asp
NM_001288607.1:c.1856+49G>T (ADAMTSL4)	NP_001275536.1:n.1856+49G>T
NM_001288608.1:c.1905G>T (ADAMTSL4)	NP_001275537.1:p.Glu635Asp
NM_019032.5:c.1836G>T (ADAMTSL4)	NP_061905.2:p.Glu612Asp
NM_025008.4:c.1836G>T (ADAMTSL4)	NP_079284.2:p.Glu612Asp
XM_011509644.1:c.2004G>T (ADAMTSL4)	XP_011507946.1:p.Glu668Asp
XM_011509645.1:c.1935G>T (ADAMTSL4)	XP_011507947.1:p.Glu645Asp
XM_011509646.1:c.1905G>T (ADAMTSL4)	XP_011507948.1:p.Glu635Asp
XM_011509647.1:c.1905G>T (ADAMTSL4)	XP_011507949.1:p.Glu635Asp
XM_011509648.1:c.1905G>T (ADAMTSL4)	XP_011507950.1:p.Glu635Asp
XM_011509649.1:c.2004G>T (ADAMTSL4)	XP_011507951.1:p.Glu668Asp
XM_011509650.1:c.2004G>T (ADAMTSL4)	XP_011507952.1:p.Glu668Asp
XM_011509651.1:c.513G>T (ADAMTSL4)	XP_011507953.1:p.Glu171Asp
XM_011509652.1:c.513G>T (ADAMTSL4)	XP_011507954.1:p.Glu171Asp
XR_921844.1:n.2189G>T (ADAMTSL4)
XR_922133.1:n.139+668C>A (ADAMTSL4-AS2)
XM_011509644.3:c.2004G>T (ADAMTSL4)	XP_011507946.1:p.Glu668Asp
XM_011509645.3:c.1935G>T (ADAMTSL4)	XP_011507947.1:p.Glu645Asp
XM_011509648.3:c.1905G>T (ADAMTSL4)	XP_011507950.1:p.Glu635Asp
XM_011509649.3:c.2004G>T (ADAMTSL4)	XP_011507951.1:p.Glu668Asp
XM_011509650.3:c.2004G>T (ADAMTSL4)	XP_011507952.1:p.Glu668Asp
XM_011509651.2:c.513G>T (ADAMTSL4)	XP_011507953.1:p.Glu171Asp
XM_011509652.2:c.513G>T (ADAMTSL4)	XP_011507954.1:p.Glu171Asp
XM_017001506.2:c.1905G>T (ADAMTSL4)	XP_016856995.1:p.Glu635Asp
XM_017001507.1:c.249G>T (ADAMTSL4)	XP_016856996.1:p.Glu83Asp
XR_001737242.2:n.1989G>T (ADAMTSL4)
XR_921844.3:n.2162G>T (ADAMTSL4)
NM_001288607.2:c.1856+49G>T (ADAMTSL4)	NP_001275536.1:n.1856+49G>T
NM_025008.5:c.1836G>T (ADAMTSL4)	NP_079284.2:p.Glu612Asp
NM_001288608.2:c.1905G>T (ADAMTSL4)	NP_001275537.1:p.Glu635Asp
NM_001378596.1:c.1836G>T (ADAMTSL4)	NP_001365525.1:p.Glu612Asp
NM_019032.6:c.1836G>T (ADAMTSL4) MANE Select	NP_061905.2:p.Glu612Asp