Canonical Allele Identifier: CA1737037592

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771912T= , CM000669.2:g.116771912T=	GRCh38
NC_000007.13:g.116411966T= , CM000669.1:g.116411966T=	GRCh37
NC_000007.12:g.116199202T=	NCBI36
NG_008996.1:g.104508T= , LRG_662:g.104508T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*556T=	ENSP00000410980.2:n.*556T=
ENST00000318493.11:c.3005T=	ENSP00000317272.6:p.Val1002=
ENST00000397752.8:c.2951T= MANE Select	ENSP00000380860.3:p.Val984=
ENST00000318493.10:c.3005T=	ENSP00000317272.6:p.Val1002=
ENST00000397752.7:c.2951T=	ENSP00000380860.3:p.Val984=
ENST00000454623.1:c.283+258T=	ENSP00000398140.1:n.283+258T=
NM_000245.2:c.2951T=	NP_000236.2:p.Val984=
NM_001127500.1:c.3005T= , LRG_662t1:c.3005T=	NP_001120972.1:p.Val1002=
XM_006715990.2:c.1661T=	XP_006716053.1:p.Val554=
XM_006715991.2:c.1661T=	XP_006716054.1:p.Val554=
XM_011516223.1:c.3008T=	XP_011514525.1:p.Val1003=
NM_000245.3:c.2951T=	NP_000236.2:p.Val984=
NM_001127500.2:c.3005T=	NP_001120972.1:p.Val1002=
NM_001324402.1:c.1661T=	NP_001311331.1:p.Val554=
XR_001744772.1:n.3082T=
NM_001127500.3:c.3005T=	NP_001120972.1:p.Val1002=
NM_000245.4:c.2951T= MANE Select	NP_000236.2:p.Val984=
NM_001324402.2:c.1661T=	NP_001311331.1:p.Val554=