Canonical Allele Identifier: CA342313357

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• MyVariant Identifiers: chr1:g.150529472C>G (hg19) ; chr1:g.150556996C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150556996C>G , CM000663.2:g.150556996C>G	GRCh38
NC_000001.10:g.150529472C>G , CM000663.1:g.150529472C>G	GRCh37
NC_000001.9:g.148796096C>G	NCBI36
NG_012172.1:g.12575C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.1807C>G (ADAMTSL4) MANE Select	ENSP00000271643.4:p.Pro603Ala
ENST00000674043.1:c.1876C>G (ADAMTSL4)	ENSP00000501295.1:p.Pro626Ala
ENST00000674058.1:c.1856+20C>G (ADAMTSL4)	ENSP00000501255.1:n.1856+20C>G
ENST00000271643.8:c.1807C>G (ADAMTSL4)	ENSP00000271643.4:p.Pro603Ala
ENST00000369038.6:c.1807C>G (ADAMTSL4)	ENSP00000358034.2:p.Pro603Ala
ENST00000369039.9:c.1876C>G (ADAMTSL4)	ENSP00000358035.5:p.Pro626Ala
ENST00000369041.9:c.1807C>G (ADAMTSL4)	ENSP00000358037.5:p.Pro603Ala
ENST00000622417.4:c.421C>G (ADAMTSL4)	ENSP00000477897.1:p.Pro141Ala
NM_001288607.1:c.1856+20C>G (ADAMTSL4)	NP_001275536.1:n.1856+20C>G
NM_001288608.1:c.1876C>G (ADAMTSL4)	NP_001275537.1:p.Pro626Ala
NM_019032.5:c.1807C>G (ADAMTSL4)	NP_061905.2:p.Pro603Ala
NM_025008.4:c.1807C>G (ADAMTSL4)	NP_079284.2:p.Pro603Ala
XM_011509644.1:c.1975C>G (ADAMTSL4)	XP_011507946.1:p.Pro659Ala
XM_011509645.1:c.1906C>G (ADAMTSL4)	XP_011507947.1:p.Pro636Ala
XM_011509646.1:c.1876C>G (ADAMTSL4)	XP_011507948.1:p.Pro626Ala
XM_011509647.1:c.1876C>G (ADAMTSL4)	XP_011507949.1:p.Pro626Ala
XM_011509648.1:c.1876C>G (ADAMTSL4)	XP_011507950.1:p.Pro626Ala
XM_011509649.1:c.1975C>G (ADAMTSL4)	XP_011507951.1:p.Pro659Ala
XM_011509650.1:c.1975C>G (ADAMTSL4)	XP_011507952.1:p.Pro659Ala
XM_011509651.1:c.484C>G (ADAMTSL4)	XP_011507953.1:p.Pro162Ala
XM_011509652.1:c.484C>G (ADAMTSL4)	XP_011507954.1:p.Pro162Ala
XR_921844.1:n.2160C>G (ADAMTSL4)
XR_922133.1:n.139+697G>C (ADAMTSL4-AS2)
XM_011509644.3:c.1975C>G (ADAMTSL4)	XP_011507946.1:p.Pro659Ala
XM_011509645.3:c.1906C>G (ADAMTSL4)	XP_011507947.1:p.Pro636Ala
XM_011509648.3:c.1876C>G (ADAMTSL4)	XP_011507950.1:p.Pro626Ala
XM_011509649.3:c.1975C>G (ADAMTSL4)	XP_011507951.1:p.Pro659Ala
XM_011509650.3:c.1975C>G (ADAMTSL4)	XP_011507952.1:p.Pro659Ala
XM_011509651.2:c.484C>G (ADAMTSL4)	XP_011507953.1:p.Pro162Ala
XM_011509652.2:c.484C>G (ADAMTSL4)	XP_011507954.1:p.Pro162Ala
XM_017001506.2:c.1876C>G (ADAMTSL4)	XP_016856995.1:p.Pro626Ala
XM_017001507.1:c.220C>G (ADAMTSL4)	XP_016856996.1:p.Pro74Ala
XR_001737242.2:n.1960C>G (ADAMTSL4)
XR_921844.3:n.2133C>G (ADAMTSL4)
NM_001288607.2:c.1856+20C>G (ADAMTSL4)	NP_001275536.1:n.1856+20C>G
NM_025008.5:c.1807C>G (ADAMTSL4)	NP_079284.2:p.Pro603Ala
NM_001288608.2:c.1876C>G (ADAMTSL4)	NP_001275537.1:p.Pro626Ala
NM_001378596.1:c.1807C>G (ADAMTSL4)	NP_001365525.1:p.Pro603Ala
NM_019032.6:c.1807C>G (ADAMTSL4) MANE Select	NP_061905.2:p.Pro603Ala