Canonical Allele Identifier: CA342313765

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• dbSNP Id: rs1214671728
• gnomAD v2: 1-150529776-T-C
• gnomAD v3: 1-150557300-T-C
• gnomAD v4: 1-150557300-T-C
• MyVariant Identifiers: chr1:g.150529776T>C (hg19) ; chr1:g.150557300T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150557300T>C , CM000663.2:g.150557300T>C	GRCh38
NC_000001.10:g.150529776T>C , CM000663.1:g.150529776T>C	GRCh37
NC_000001.9:g.148796400T>C	NCBI36
NG_012172.1:g.12879T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.2012T>C (ADAMTSL4) MANE Select	ENSP00000271643.4:p.Val671Ala
ENST00000674043.1:c.2081T>C (ADAMTSL4)	ENSP00000501295.1:p.Val694Ala
ENST00000674058.1:c.1895T>C (ADAMTSL4)	ENSP00000501255.1:p.Val632Ala
ENST00000271643.8:c.2012T>C (ADAMTSL4)	ENSP00000271643.4:p.Val671Ala
ENST00000369038.6:c.2012T>C (ADAMTSL4)	ENSP00000358034.2:p.Val671Ala
ENST00000369039.9:c.2081T>C (ADAMTSL4)	ENSP00000358035.5:p.Val694Ala
ENST00000369041.9:c.2012T>C (ADAMTSL4)	ENSP00000358037.5:p.Val671Ala
ENST00000622417.4:c.626T>C (ADAMTSL4)	ENSP00000477897.1:p.Val209Ala
NM_001288607.1:c.1895T>C (ADAMTSL4)	NP_001275536.1:p.Val632Ala
NM_001288608.1:c.2081T>C (ADAMTSL4)	NP_001275537.1:p.Val694Ala
NM_019032.5:c.2012T>C (ADAMTSL4)	NP_061905.2:p.Val671Ala
NM_025008.4:c.2012T>C (ADAMTSL4)	NP_079284.2:p.Val671Ala
XM_011509644.1:c.2180T>C (ADAMTSL4)	XP_011507946.1:p.Val727Ala
XM_011509645.1:c.2111T>C (ADAMTSL4)	XP_011507947.1:p.Val704Ala
XM_011509646.1:c.2081T>C (ADAMTSL4)	XP_011507948.1:p.Val694Ala
XM_011509647.1:c.2081T>C (ADAMTSL4)	XP_011507949.1:p.Val694Ala
XM_011509648.1:c.2081T>C (ADAMTSL4)	XP_011507950.1:p.Val694Ala
XM_011509649.1:c.2180T>C (ADAMTSL4)	XP_011507951.1:p.Val727Ala
XM_011509650.1:c.2180T>C (ADAMTSL4)	XP_011507952.1:p.Val727Ala
XM_011509651.1:c.689T>C (ADAMTSL4)	XP_011507953.1:p.Val230Ala
XM_011509652.1:c.689T>C (ADAMTSL4)	XP_011507954.1:p.Val230Ala
XR_921844.1:n.2365T>C (ADAMTSL4)
XR_922133.1:n.139+393A>G (ADAMTSL4-AS2)
XM_011509644.3:c.2180T>C (ADAMTSL4)	XP_011507946.1:p.Val727Ala
XM_011509645.3:c.2111T>C (ADAMTSL4)	XP_011507947.1:p.Val704Ala
XM_011509648.3:c.2081T>C (ADAMTSL4)	XP_011507950.1:p.Val694Ala
XM_011509649.3:c.2180T>C (ADAMTSL4)	XP_011507951.1:p.Val727Ala
XM_011509650.3:c.2180T>C (ADAMTSL4)	XP_011507952.1:p.Val727Ala
XM_011509651.2:c.689T>C (ADAMTSL4)	XP_011507953.1:p.Val230Ala
XM_011509652.2:c.689T>C (ADAMTSL4)	XP_011507954.1:p.Val230Ala
XM_017001506.2:c.2081T>C (ADAMTSL4)	XP_016856995.1:p.Val694Ala
XM_017001507.1:c.425T>C (ADAMTSL4)	XP_016856996.1:p.Val142Ala
XR_001737242.2:n.2165T>C (ADAMTSL4)
XR_921844.3:n.2338T>C (ADAMTSL4)
NM_001288607.2:c.1895T>C (ADAMTSL4)	NP_001275536.1:p.Val632Ala
NM_025008.5:c.2012T>C (ADAMTSL4)	NP_079284.2:p.Val671Ala
NM_001288608.2:c.2081T>C (ADAMTSL4)	NP_001275537.1:p.Val694Ala
NM_001378596.1:c.2012T>C (ADAMTSL4)	NP_001365525.1:p.Val671Ala
NM_019032.6:c.2012T>C (ADAMTSL4) MANE Select	NP_061905.2:p.Val671Ala