Canonical Allele Identifier: CA2479212206

Gene: ADAMTSL4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150560360T= , CM000663.2:g.150560360T=	GRCh38
NC_000001.10:g.150532836T= , CM000663.1:g.150532836T=	GRCh37
NC_000001.9:g.148799460T=	NCBI36
NG_012172.1:g.15939T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000271643.9:c.*164T= MANE Select	ENSP00000271643.4:n.*164T=
ENST00000674043.1:c.*164T=	ENSP00000501295.1:n.*164T=
ENST00000674058.1:c.*164T=	ENSP00000501255.1:n.*164T=
ENST00000271643.8:c.*164T=	ENSP00000271643.4:n.*164T=
ENST00000369038.6:c.*164T=	ENSP00000358034.2:n.*164T=
ENST00000369039.9:c.*164T=	ENSP00000358035.5:n.*164T=
ENST00000489159.1:n.1226T=
ENST00000622417.4:c.*693T=	ENSP00000477897.1:n.*693T=
NM_001288607.1:c.*164T=	NP_001275536.1:n.*164T=
NM_001288608.1:c.*164T=	NP_001275537.1:n.*164T=
NM_019032.5:c.*164T=	NP_061905.2:n.*164T=
XM_011509644.1:c.*164T=	XP_011507946.1:n.*164T=
XM_011509645.1:c.*164T=	XP_011507947.1:n.*164T=
XM_011509646.1:c.*164T=	XP_011507948.1:n.*164T=
XM_011509647.1:c.*164T=	XP_011507949.1:n.*164T=
XM_011509648.1:c.*164T=	XP_011507950.1:n.*164T=
XM_011509651.1:c.*164T=	XP_011507953.1:n.*164T=
XM_011509652.1:c.*164T=	XP_011507954.1:n.*164T=
XR_921844.1:n.3958T=
XM_011509644.3:c.*164T=	XP_011507946.1:n.*164T=
XM_011509645.3:c.*164T=	XP_011507947.1:n.*164T=
XM_011509648.3:c.*164T=	XP_011507950.1:n.*164T=
XM_011509651.2:c.*164T=	XP_011507953.1:n.*164T=
XM_011509652.2:c.*164T=	XP_011507954.1:n.*164T=
XM_017001506.2:c.*164T=	XP_016856995.1:n.*164T=
XM_017001507.1:c.*164T=	XP_016856996.1:n.*164T=
XR_921844.3:n.3931T=
NM_001288607.2:c.*164T=	NP_001275536.1:n.*164T=
NM_001288608.2:c.*164T=	NP_001275537.1:n.*164T=
NM_001378596.1:c.*164T=	NP_001365525.1:n.*164T=
NM_019032.6:c.*164T= MANE Select	NP_061905.2:n.*164T=