Canonical Allele Identifier: CA1737025344

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759419A= , CM000669.2:g.116759419A=	GRCh38
NC_000007.13:g.116399473A= , CM000669.1:g.116399473A=	GRCh37
NC_000007.12:g.116186709A=	NCBI36
NG_008996.1:g.92015A= , LRG_662:g.92015A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2293A=	ENSP00000398776.2:p.Lys765=
ENST00000436117.3:c.2264+799A=	ENSP00000410980.2:n.2264+799A=
ENST00000318493.11:c.2347A=	ENSP00000317272.6:p.Lys783=
ENST00000397752.8:c.2293A= MANE Select	ENSP00000380860.3:p.Lys765=
ENST00000318493.10:c.2347A=	ENSP00000317272.6:p.Lys783=
ENST00000397752.7:c.2293A=	ENSP00000380860.3:p.Lys765=
ENST00000422097.1:c.133A=	ENSP00000398776.1:p.Lys45=
ENST00000436117.2:c.2264+799A=	ENSP00000410980.2:n.2264+799A=
NM_000245.2:c.2293A=	NP_000236.2:p.Lys765=
NM_001127500.1:c.2347A= , LRG_662t1:c.2347A=	NP_001120972.1:p.Lys783=
XM_006715990.2:c.1003A=	XP_006716053.1:p.Lys335=
XM_006715991.2:c.1003A=	XP_006716054.1:p.Lys335=
XM_011516223.1:c.2350A=	XP_011514525.1:p.Lys784=
NM_000245.3:c.2293A=	NP_000236.2:p.Lys765=
NM_001127500.2:c.2347A=	NP_001120972.1:p.Lys783=
NM_001324401.1:c.2293A=	NP_001311330.1:p.Lys765=
NM_001324402.1:c.1003A=	NP_001311331.1:p.Lys335=
XR_001744772.1:n.2495+799A=
NM_001127500.3:c.2347A=	NP_001120972.1:p.Lys783=
NM_000245.4:c.2293A= MANE Select	NP_000236.2:p.Lys765=
NM_001324401.2:c.2293A=	NP_001311330.1:p.Lys765=
NM_001324402.2:c.1003A=	NP_001311331.1:p.Lys335=
NM_001324401.3:c.2293A=	NP_001311330.1:p.Lys765=