Canonical Allele Identifier: CA10607807

Gene: ADAMTSL4 ADAMTSL4-AS2

Linked Data

• ClinVar Variation Id: 292514
• ClinVar RCV Id: RCV000355471
• dbSNP Id: rs886045266
• gnomAD v3: 1-150549880-G-A
• gnomAD v4: 1-150549880-G-A
• MyVariant Identifiers: chr1:g.150522356G>A (hg19) ; chr1:g.150549880G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150549880G>A , CM000663.2:g.150549880G>A	GRCh38
NC_000001.10:g.150522356G>A , CM000663.1:g.150522356G>A	GRCh37
NC_000001.9:g.148788980G>A	NCBI36
NG_012172.1:g.5459G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.-100G>A (ADAMTSL4) MANE Select	ENSP00000271643.4:n.-100G>A
ENST00000674043.1:c.-100G>A (ADAMTSL4)	ENSP00000501295.1:n.-100G>A
ENST00000674058.1:c.-100G>A (ADAMTSL4)	ENSP00000501255.1:n.-100G>A
ENST00000271643.8:c.-100G>A (ADAMTSL4)	ENSP00000271643.4:n.-100G>A
ENST00000369039.9:c.-100G>A (ADAMTSL4)	ENSP00000358035.5:n.-100G>A
ENST00000369041.9:c.-100G>A (ADAMTSL4)	ENSP00000358037.5:n.-100G>A
ENST00000483335.1:n.138G>A (ADAMTSL4)
NM_001288607.1:c.-100G>A (ADAMTSL4)	NP_001275536.1:n.-100G>A
NM_001288608.1:c.-100G>A (ADAMTSL4)	NP_001275537.1:n.-100G>A
NM_019032.5:c.-100G>A (ADAMTSL4)	NP_061905.2:n.-100G>A
NM_025008.4:c.-100G>A (ADAMTSL4)	NP_079284.2:n.-100G>A
XM_011509646.1:c.-235G>A (ADAMTSL4)	XP_011507948.1:n.-235G>A
XM_011509648.1:c.-85+381G>A (ADAMTSL4)	XP_011507950.1:n.-85+381G>A
XR_922132.1:n.371-1130C>T (ADAMTSL4-AS2)
XR_922133.1:n.418-1130C>T (ADAMTSL4-AS2)
XM_011509648.3:c.-85+381G>A (ADAMTSL4)	XP_011507950.1:n.-85+381G>A
XM_017001506.2:c.-481G>A (ADAMTSL4)	XP_016856995.1:n.-481G>A
XR_001738227.1:n.467-1130C>T (ADAMTSL4-AS2)
XR_001738229.1:n.358-1130C>T (ADAMTSL4-AS2)
NM_001288607.2:c.-100G>A (ADAMTSL4)	NP_001275536.1:n.-100G>A
NM_025008.5:c.-100G>A (ADAMTSL4)	NP_079284.2:n.-100G>A
NM_001288608.2:c.-100G>A (ADAMTSL4)	NP_001275537.1:n.-100G>A
NM_001378596.1:c.-481G>A (ADAMTSL4)	NP_001365525.1:n.-481G>A
NM_019032.6:c.-100G>A (ADAMTSL4) MANE Select	NP_061905.2:n.-100G>A