Canonical Allele Identifier: CA30074029

Gene: ADAMTSL4

Linked Data

• dbSNP Id: rs756753622
• gnomAD v3: 1-150560362-T-C
• gnomAD v4: 1-150560362-T-C
• MyVariant Identifiers: chr1:g.150532838T>C (hg19) ; chr1:g.150560362T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150560362T>C , CM000663.2:g.150560362T>C	GRCh38
NC_000001.10:g.150532838T>C , CM000663.1:g.150532838T>C	GRCh37
NC_000001.9:g.148799462T>C	NCBI36
NG_012172.1:g.15941T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.*166T>C MANE Select	ENSP00000271643.4:n.*166T>C
ENST00000674043.1:c.*166T>C	ENSP00000501295.1:n.*166T>C
ENST00000674058.1:c.*166T>C	ENSP00000501255.1:n.*166T>C
ENST00000271643.8:c.*166T>C	ENSP00000271643.4:n.*166T>C
ENST00000369038.6:c.*166T>C	ENSP00000358034.2:n.*166T>C
ENST00000369039.9:c.*166T>C	ENSP00000358035.5:n.*166T>C
ENST00000489159.1:n.1228T>C
ENST00000622417.4:c.*695T>C	ENSP00000477897.1:n.*695T>C
NM_001288607.1:c.*166T>C	NP_001275536.1:n.*166T>C
NM_001288608.1:c.*166T>C	NP_001275537.1:n.*166T>C
NM_019032.5:c.*166T>C	NP_061905.2:n.*166T>C
XM_011509644.1:c.*166T>C	XP_011507946.1:n.*166T>C
XM_011509645.1:c.*166T>C	XP_011507947.1:n.*166T>C
XM_011509646.1:c.*166T>C	XP_011507948.1:n.*166T>C
XM_011509647.1:c.*166T>C	XP_011507949.1:n.*166T>C
XM_011509648.1:c.*166T>C	XP_011507950.1:n.*166T>C
XM_011509651.1:c.*166T>C	XP_011507953.1:n.*166T>C
XM_011509652.1:c.*166T>C	XP_011507954.1:n.*166T>C
XR_921844.1:n.3960T>C
XM_011509644.3:c.*166T>C	XP_011507946.1:n.*166T>C
XM_011509645.3:c.*166T>C	XP_011507947.1:n.*166T>C
XM_011509648.3:c.*166T>C	XP_011507950.1:n.*166T>C
XM_011509651.2:c.*166T>C	XP_011507953.1:n.*166T>C
XM_011509652.2:c.*166T>C	XP_011507954.1:n.*166T>C
XM_017001506.2:c.*166T>C	XP_016856995.1:n.*166T>C
XM_017001507.1:c.*166T>C	XP_016856996.1:n.*166T>C
XR_921844.3:n.3933T>C
NM_001288607.2:c.*166T>C	NP_001275536.1:n.*166T>C
NM_001288608.2:c.*166T>C	NP_001275537.1:n.*166T>C
NM_001378596.1:c.*166T>C	NP_001365525.1:n.*166T>C
NM_019032.6:c.*166T>C MANE Select	NP_061905.2:n.*166T>C