Canonical Allele Identifier: CA1737014335

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783355C= , CM000669.2:g.116783355C=	GRCh38
NC_000007.13:g.116423409C= , CM000669.1:g.116423409C=	GRCh37
NC_000007.12:g.116210645C=	NCBI36
NG_008996.1:g.115951C= , LRG_662:g.115951C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1289C=	ENSP00000410980.2:n.*1289C=
ENST00000318493.11:c.3738C=	ENSP00000317272.6:p.Asp1246=
ENST00000397752.8:c.3684C= MANE Select	ENSP00000380860.3:p.Asp1228=
ENST00000318493.10:c.3738C=	ENSP00000317272.6:p.Asp1246=
ENST00000397752.7:c.3684C=	ENSP00000380860.3:p.Asp1228=
NM_000245.2:c.3684C=	NP_000236.2:p.Asp1228=
NM_001127500.1:c.3738C= , LRG_662t1:c.3738C=	NP_001120972.1:p.Asp1246=
XM_006715990.2:c.2394C=	XP_006716053.1:p.Asp798=
XM_006715991.2:c.2394C=	XP_006716054.1:p.Asp798=
XM_011516223.1:c.3741C=	XP_011514525.1:p.Asp1247=
NM_000245.3:c.3684C=	NP_000236.2:p.Asp1228=
NM_001127500.2:c.3738C=	NP_001120972.1:p.Asp1246=
NM_001324402.1:c.2394C=	NP_001311331.1:p.Asp798=
XR_001744772.1:n.3815C=
NM_001127500.3:c.3738C=	NP_001120972.1:p.Asp1246=
NM_000245.4:c.3684C= MANE Select	NP_000236.2:p.Asp1228=
NM_001324402.2:c.2394C=	NP_001311331.1:p.Asp798=