Canonical Allele Identifier: CA1737018747

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116755394_116755397delinsCTGA , CM000669.2:g.116755394_116755397delinsCTGA	GRCh38
NC_000007.13:g.116395448_116395451delinsCTGA , CM000669.1:g.116395448_116395451delinsCTGA	GRCh37
NC_000007.12:g.116182684_116182687delinsCTGA	NCBI36
NG_008996.1:g.87990_87993delinsCTGA , LRG_662:g.87990_87993delinsCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1741_1744delinsCTGA	ENSP00000398776.2:p.Leu581=
ENST00000436117.3:c.1741_1744delinsCTGA	ENSP00000410980.2:p.Leu581=
ENST00000318493.11:c.1741_1744delinsCTGA	ENSP00000317272.6:p.Leu581=
ENST00000397752.8:c.1741_1744delinsCTGA MANE Select	ENSP00000380860.3:p.Leu581=
ENST00000318493.10:c.1741_1744delinsCTGA	ENSP00000317272.6:p.Leu581=
ENST00000397752.7:c.1741_1744delinsCTGA	ENSP00000380860.3:p.Leu581=
ENST00000436117.2:c.1741_1744delinsCTGA	ENSP00000410980.2:p.Leu581=
ENST00000495962.1:n.721_724delinsCTGA
NM_000245.2:c.1741_1744delinsCTGA	NP_000236.2:p.Leu581=
NM_001127500.1:c.1741_1744delinsCTGA , LRG_662t1:c.1741_1744delinsCTGA	NP_001120972.1:p.Leu581=
XM_006715990.2:c.451_454delinsCTGA	XP_006716053.1:p.Leu151=
XM_006715991.2:c.451_454delinsCTGA	XP_006716054.1:p.Leu151=
XM_011516223.1:c.1798_1801delinsCTGA	XP_011514525.1:p.Leu600=
NM_000245.3:c.1741_1744delinsCTGA	NP_000236.2:p.Leu581=
NM_001127500.2:c.1741_1744delinsCTGA	NP_001120972.1:p.Leu581=
NM_001324401.1:c.1741_1744delinsCTGA	NP_001311330.1:p.Leu581=
NM_001324402.1:c.451_454delinsCTGA	NP_001311331.1:p.Leu151=
XR_001744772.1:n.1972_1975delinsCTGA
NM_001127500.3:c.1741_1744delinsCTGA	NP_001120972.1:p.Leu581=
NM_000245.4:c.1741_1744delinsCTGA MANE Select	NP_000236.2:p.Leu581=
NM_001324401.2:c.1741_1744delinsCTGA	NP_001311330.1:p.Leu581=
NM_001324402.2:c.451_454delinsCTGA	NP_001311331.1:p.Leu151=
NM_001324401.3:c.1741_1744delinsCTGA	NP_001311330.1:p.Leu581=