Canonical Allele Identifier: CA1882725543

Gene: ADAMTSL2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133570501G= , CM000671.2:g.133570501G=	GRCh38
NC_000009.11:g.136435623G= , CM000671.1:g.136435623G=	GRCh37
NC_000009.10:g.135425444G=	NCBI36
NG_009931.1:g.43338G=

Transcript Alleles

HGVS	Amino-acid Change
NM_014694.4:c.2586G= MANE Select	NP_055509.2:p.Trp862=
ENST00000651351.2:c.2586G= MANE Select	ENSP00000498961.2:p.Trp862=
NM_001145320.1:c.2586G=	NP_001138792.1:p.Trp862=
NM_001145320.2:c.2586G=	NP_001138792.1:p.Trp862=
NM_014694.3:c.2586G=	NP_055509.2:p.Trp862=
ENST00000354484.8:c.2586G=	ENSP00000346478.4:p.Trp862=
ENST00000393060.1:c.2586G=	ENSP00000376780.1:p.Trp862=
ENST00000393061.7:c.2913G=	ENSP00000376781.3:p.Trp971=
XM_005272237.2:c.2913G=	XP_005272294.1:p.Trp971=
XM_005272237.3:c.2913G=	XP_005272294.1:p.Trp971=
XM_005272238.2:c.2616G=	XP_005272295.1:p.Trp872=
XM_005272238.3:c.2616G=	XP_005272295.1:p.Trp872=
XM_005272239.2:c.2586G=	XP_005272296.1:p.Trp862=
XM_006717337.2:c.2586G=	XP_006717400.1:p.Trp862=
XM_011519241.1:c.2469G=	XP_011517543.1:p.Trp823=
XM_011519241.2:c.2796G=	XP_011517543.2:p.Trp932=
XM_011519242.1:c.2652G=	XP_011517544.1:p.Trp884=
XM_011519242.3:c.2652G=	XP_011517544.1:p.Trp884=