Canonical Allele Identifier: CA1737004022

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116706549G= , CM000669.2:g.116706549G=	GRCh38
NC_000007.13:g.116346603G= , CM000669.1:g.116346603G=	GRCh37
NC_000007.12:g.116133839G=	NCBI36
NG_008996.1:g.39145G= , LRG_662:g.39145G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.1200+6265G= MANE Select	NP_000236.2:n.1200+6265G=
ENST00000397752.8:c.1200+6265G= MANE Select	ENSP00000380860.3:n.1200+6265G=
NM_000245.2:c.1200+6265G=	NP_000236.2:n.1200+6265G=
NM_000245.3:c.1200+6265G=	NP_000236.2:n.1200+6265G=
NM_001127500.1:c.1200+6265G= , LRG_662t1:c.1200+6265G=	NP_001120972.1:n.1200+6265G=
NM_001127500.2:c.1200+6265G=	NP_001120972.1:n.1200+6265G=
NM_001127500.3:c.1200+6265G=	NP_001120972.1:n.1200+6265G=
NM_001324401.1:c.1200+6265G=	NP_001311330.1:n.1200+6265G=
NM_001324401.2:c.1200+6265G=	NP_001311330.1:n.1200+6265G=
NM_001324401.3:c.1200+6265G=	NP_001311330.1:n.1200+6265G=
NM_001324402.1:c.-90-25119G=	NP_001311331.1:n.-90-25119G=
NM_001324402.2:c.-90-25119G=	NP_001311331.1:n.-90-25119G=
ENST00000318493.10:c.1200+6265G=	ENSP00000317272.6:n.1200+6265G=
ENST00000318493.11:c.1200+6265G=	ENSP00000317272.6:n.1200+6265G=
ENST00000397752.7:c.1200+6265G=	ENSP00000380860.3:n.1200+6265G=
ENST00000422097.2:c.1200+6265G=	ENSP00000398776.2:n.1200+6265G=
ENST00000436117.2:c.1200+6265G=	ENSP00000410980.2:n.1200+6265G=
ENST00000436117.3:c.1200+6265G=	ENSP00000410980.2:n.1200+6265G=
XM_006715991.2:c.-90-25119G=	XP_006716054.1:n.-90-25119G=
XM_011516223.1:c.1257+6265G=	XP_011514525.1:n.1257+6265G=
XR_001744772.1:n.1431+6265G=