Canonical Allele Identifier: CA2479211603

Gene: ADAMTSL4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.150558996G= , CM000663.2:g.150558996G=	GRCh38
NC_000001.10:g.150531472G= , CM000663.1:g.150531472G=	GRCh37
NC_000001.9:g.148798096G=	NCBI36
NG_012172.1:g.14575G=

Transcript Alleles

HGVS	Amino-acid Change
NM_019032.6:c.2594G= MANE Select	NP_061905.2:p.Arg865=
ENST00000271643.9:c.2594G= MANE Select	ENSP00000271643.4:p.Arg865=
NM_001288607.1:c.2477G=	NP_001275536.1:p.Arg826=
NM_001288607.2:c.2477G=	NP_001275536.1:p.Arg826=
NM_001288608.1:c.2663G=	NP_001275537.1:p.Arg888=
NM_001288608.2:c.2663G=	NP_001275537.1:p.Arg888=
NM_001378596.1:c.2594G=	NP_001365525.1:p.Arg865=
NM_019032.5:c.2594G=	NP_061905.2:p.Arg865=
ENST00000271643.8:c.2594G=	ENSP00000271643.4:p.Arg865=
ENST00000369038.6:c.2594G=	ENSP00000358034.2:p.Arg865=
ENST00000369039.9:c.2663G=	ENSP00000358035.5:p.Arg888=
ENST00000489159.1:n.431G=
ENST00000622417.4:c.1208G=	ENSP00000477897.1:p.Arg403=
ENST00000674043.1:c.2663G=	ENSP00000501295.1:p.Arg888=
ENST00000674058.1:c.2477G=	ENSP00000501255.1:p.Arg826=
XM_011509644.1:c.2762G=	XP_011507946.1:p.Arg921=
XM_011509644.3:c.2762G=	XP_011507946.1:p.Arg921=
XM_011509645.1:c.2693G=	XP_011507947.1:p.Arg898=
XM_011509645.3:c.2693G=	XP_011507947.1:p.Arg898=
XM_011509646.1:c.2663G=	XP_011507948.1:p.Arg888=
XM_011509647.1:c.2663G=	XP_011507949.1:p.Arg888=
XM_011509648.1:c.2663G=	XP_011507950.1:p.Arg888=
XM_011509648.3:c.2663G=	XP_011507950.1:p.Arg888=
XM_011509651.1:c.1271G=	XP_011507953.1:p.Arg424=
XM_011509651.2:c.1271G=	XP_011507953.1:p.Arg424=
XM_011509652.1:c.1271G=	XP_011507954.1:p.Arg424=
XM_011509652.2:c.1271G=	XP_011507954.1:p.Arg424=
XM_017001506.2:c.2663G=	XP_016856995.1:p.Arg888=
XM_017001507.1:c.1007G=	XP_016856996.1:p.Arg336=
XR_921844.1:n.3163G=
XR_921844.3:n.3136G=