Canonical Allele Identifier: CA1737037603

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771932C= , CM000669.2:g.116771932C=	GRCh38
NC_000007.13:g.116411986C= , CM000669.1:g.116411986C=	GRCh37
NC_000007.12:g.116199222C=	NCBI36
NG_008996.1:g.104528C= , LRG_662:g.104528C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*576C=	ENSP00000410980.2:n.*576C=
ENST00000318493.11:c.3025C=	ENSP00000317272.6:p.Pro1009=
ENST00000397752.8:c.2971C= MANE Select	ENSP00000380860.3:p.Pro991=
ENST00000318493.10:c.3025C=	ENSP00000317272.6:p.Pro1009=
ENST00000397752.7:c.2971C=	ENSP00000380860.3:p.Pro991=
ENST00000454623.1:c.283+278C=	ENSP00000398140.1:n.283+278C=
NM_000245.2:c.2971C=	NP_000236.2:p.Pro991=
NM_001127500.1:c.3025C= , LRG_662t1:c.3025C=	NP_001120972.1:p.Pro1009=
XM_006715990.2:c.1681C=	XP_006716053.1:p.Pro561=
XM_006715991.2:c.1681C=	XP_006716054.1:p.Pro561=
XM_011516223.1:c.3028C=	XP_011514525.1:p.Pro1010=
NM_000245.3:c.2971C=	NP_000236.2:p.Pro991=
NM_001127500.2:c.3025C=	NP_001120972.1:p.Pro1009=
NM_001324402.1:c.1681C=	NP_001311331.1:p.Pro561=
XR_001744772.1:n.3102C=
NM_001127500.3:c.3025C=	NP_001120972.1:p.Pro1009=
NM_000245.4:c.2971C= MANE Select	NP_000236.2:p.Pro991=
NM_001324402.2:c.1681C=	NP_001311331.1:p.Pro561=