Canonical Allele Identifier: CA2746064361

Gene: ADAMTSL4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150560391T>A , CM000663.2:g.150560391T>A	GRCh38
NC_000001.10:g.150532867T>A , CM000663.1:g.150532867T>A	GRCh37
NC_000001.9:g.148799491T>A	NCBI36
NG_012172.1:g.15970T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.*195T>A MANE Select	ENSP00000271643.4:n.*195T>A
ENST00000674043.1:c.*195T>A	ENSP00000501295.1:n.*195T>A
ENST00000674058.1:c.*195T>A	ENSP00000501255.1:n.*195T>A
ENST00000271643.8:c.*195T>A	ENSP00000271643.4:n.*195T>A
ENST00000369038.6:c.*195T>A	ENSP00000358034.2:n.*195T>A
ENST00000369039.9:c.*195T>A	ENSP00000358035.5:n.*195T>A
ENST00000489159.1:n.1257T>A
ENST00000622417.4:c.*724T>A	ENSP00000477897.1:n.*724T>A
NM_001288607.1:c.*195T>A	NP_001275536.1:n.*195T>A
NM_001288608.1:c.*195T>A	NP_001275537.1:n.*195T>A
NM_019032.5:c.*195T>A	NP_061905.2:n.*195T>A
XM_011509644.1:c.*195T>A	XP_011507946.1:n.*195T>A
XM_011509645.1:c.*195T>A	XP_011507947.1:n.*195T>A
XM_011509646.1:c.*195T>A	XP_011507948.1:n.*195T>A
XM_011509647.1:c.*195T>A	XP_011507949.1:n.*195T>A
XM_011509648.1:c.*195T>A	XP_011507950.1:n.*195T>A
XM_011509651.1:c.*195T>A	XP_011507953.1:n.*195T>A
XM_011509652.1:c.*195T>A	XP_011507954.1:n.*195T>A
XR_921844.1:n.3989T>A
XM_011509644.3:c.*195T>A	XP_011507946.1:n.*195T>A
XM_011509645.3:c.*195T>A	XP_011507947.1:n.*195T>A
XM_011509648.3:c.*195T>A	XP_011507950.1:n.*195T>A
XM_011509651.2:c.*195T>A	XP_011507953.1:n.*195T>A
XM_011509652.2:c.*195T>A	XP_011507954.1:n.*195T>A
XM_017001506.2:c.*195T>A	XP_016856995.1:n.*195T>A
XM_017001507.1:c.*195T>A	XP_016856996.1:n.*195T>A
XR_921844.3:n.3962T>A
NM_001288607.2:c.*195T>A	NP_001275536.1:n.*195T>A
NM_001288608.2:c.*195T>A	NP_001275537.1:n.*195T>A
NM_001378596.1:c.*195T>A	NP_001365525.1:n.*195T>A
NM_019032.6:c.*195T>A MANE Select	NP_061905.2:n.*195T>A