Canonical Allele Identifier: CA2192014998

Gene: ADAMTSL3

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.83854003C= , CM000677.2:g.83854003C=	GRCh38
NC_000015.9:g.84522755C= , CM000677.1:g.84522755C=	GRCh37
NC_000015.8:g.82313759C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_207517.3:c.728-4763C= MANE Select	NP_997400.2:n.728-4763C=
ENST00000286744.10:c.728-4763C= MANE Select	ENSP00000286744.5:n.728-4763C=
NM_001301110.1:c.728-4763C=	NP_001288039.1:n.728-4763C=
NM_001301110.2:c.728-4763C=	NP_001288039.1:n.728-4763C=
NM_207517.2:c.728-4763C=	NP_997400.2:n.728-4763C=
ENST00000286744.9:c.728-4763C=	ENSP00000286744.5:n.728-4763C=
ENST00000561483.5:n.943-4763C=
ENST00000567476.1:c.728-4763C=	ENSP00000456313.1:n.728-4763C=
ENST00000569510.5:n.943-4763C=
XM_011521821.1:c.808+4281C=	XP_011520123.1:n.808+4281C=
XM_011521822.1:c.808+4281C=	XP_011520124.1:n.808+4281C=
XM_011521822.2:c.808+4281C=	XP_011520124.1:n.808+4281C=
XM_011521823.1:c.808+4281C=	XP_011520125.1:n.808+4281C=
XM_011521823.2:c.808+4281C=	XP_011520125.1:n.808+4281C=
XM_011521824.1:c.808+4281C=	XP_011520126.1:n.808+4281C=
XM_011521824.2:c.808+4281C=	XP_011520126.1:n.808+4281C=
XM_011521825.1:c.808+4281C=	XP_011520127.1:n.808+4281C=
XM_011521825.2:c.808+4281C=	XP_011520127.1:n.808+4281C=
XM_017022434.1:c.808+4281C=	XP_016877923.1:n.808+4281C=
XM_017022435.1:c.232+4281C=	XP_016877924.1:n.232+4281C=
XM_024450000.1:c.808+4281C=	XP_024305768.1:n.808+4281C=
XR_931873.1:n.841+4281C=
XR_931873.2:n.1023+4281C=