Canonical Allele Identifier: CA1737025487

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759465A= , CM000669.2:g.116759465A=	GRCh38
NC_000007.13:g.116399519A= , CM000669.1:g.116399519A=	GRCh37
NC_000007.12:g.116186755A=	NCBI36
NG_008996.1:g.92061A= , LRG_662:g.92061A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2339A=	ENSP00000398776.2:p.His780=
ENST00000436117.3:c.2264+845A=	ENSP00000410980.2:n.2264+845A=
ENST00000318493.11:c.2393A=	ENSP00000317272.6:p.His798=
ENST00000397752.8:c.2339A= MANE Select	ENSP00000380860.3:p.His780=
ENST00000318493.10:c.2393A=	ENSP00000317272.6:p.His798=
ENST00000397752.7:c.2339A=	ENSP00000380860.3:p.His780=
ENST00000422097.1:c.179A=	ENSP00000398776.1:p.His60=
ENST00000436117.2:c.2264+845A=	ENSP00000410980.2:n.2264+845A=
NM_000245.2:c.2339A=	NP_000236.2:p.His780=
NM_001127500.1:c.2393A= , LRG_662t1:c.2393A=	NP_001120972.1:p.His798=
XM_006715990.2:c.1049A=	XP_006716053.1:p.His350=
XM_006715991.2:c.1049A=	XP_006716054.1:p.His350=
XM_011516223.1:c.2396A=	XP_011514525.1:p.His799=
NM_000245.3:c.2339A=	NP_000236.2:p.His780=
NM_001127500.2:c.2393A=	NP_001120972.1:p.His798=
NM_001324401.1:c.2339A=	NP_001311330.1:p.His780=
NM_001324402.1:c.1049A=	NP_001311331.1:p.His350=
XR_001744772.1:n.2495+845A=
NM_001127500.3:c.2393A=	NP_001120972.1:p.His798=
NM_000245.4:c.2339A= MANE Select	NP_000236.2:p.His780=
NM_001324401.2:c.2339A=	NP_001311330.1:p.His780=
NM_001324402.2:c.1049A=	NP_001311331.1:p.His350=
NM_001324401.3:c.2339A=	NP_001311330.1:p.His780=