Canonical Allele Identifier: CA1882728663

Gene: ADAMTSL2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133540625C= , CM000671.2:g.133540625C=	GRCh38
NC_000009.11:g.136405747C= , CM000671.1:g.136405747C=	GRCh37
NC_000009.10:g.135395568C=	NCBI36
NG_009931.1:g.13462C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651351.2:c.440C= MANE Select	ENSP00000498961.2:p.Pro147=
ENST00000354484.8:c.440C=	ENSP00000346478.4:p.Pro147=
ENST00000393060.1:c.440C=	ENSP00000376780.1:p.Pro147=
ENST00000393061.7:c.767C=	ENSP00000376781.3:p.Pro256=
NM_001145320.1:c.440C=	NP_001138792.1:p.Pro147=
NM_014694.3:c.440C=	NP_055509.2:p.Pro147=
XM_005272237.2:c.767C=	XP_005272294.1:p.Pro256=
XM_005272238.2:c.475C=	XP_005272295.1:p.Arg159=
XM_005272239.2:c.440C=	XP_005272296.1:p.Pro147=
XM_006717337.2:c.440C=	XP_006717400.1:p.Pro147=
XM_011519241.1:c.328C=	XP_011517543.1:p.Arg110=
XM_011519242.1:c.506C=	XP_011517544.1:p.Pro169=
XM_005272237.3:c.767C=	XP_005272294.1:p.Pro256=
XM_005272238.3:c.475C=	XP_005272295.1:p.Arg159=
XM_011519241.2:c.655C=	XP_011517543.2:p.Arg219=
XM_011519242.3:c.506C=	XP_011517544.1:p.Pro169=
NM_014694.4:c.440C= MANE Select	NP_055509.2:p.Pro147=
NM_001145320.2:c.440C=	NP_001138792.1:p.Pro147=