Canonical Allele Identifier: CA1737037445

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771623C= , CM000669.2:g.116771623C=	GRCh38
NC_000007.13:g.116411677C= , CM000669.1:g.116411677C=	GRCh37
NC_000007.12:g.116198913C=	NCBI36
NG_008996.1:g.104219C= , LRG_662:g.104219C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*461C=	ENSP00000410980.2:n.*461C=
ENST00000318493.11:c.2910C=	ENSP00000317272.6:p.Phe970=
ENST00000397752.8:c.2856C= MANE Select	ENSP00000380860.3:p.Phe952=
ENST00000318493.10:c.2910C=	ENSP00000317272.6:p.Phe970=
ENST00000397752.7:c.2856C=	ENSP00000380860.3:p.Phe952=
ENST00000454623.1:c.252C=	ENSP00000398140.1:p.Phe84=
NM_000245.2:c.2856C=	NP_000236.2:p.Phe952=
NM_001127500.1:c.2910C= , LRG_662t1:c.2910C=	NP_001120972.1:p.Phe970=
XM_006715990.2:c.1566C=	XP_006716053.1:p.Phe522=
XM_006715991.2:c.1566C=	XP_006716054.1:p.Phe522=
XM_011516223.1:c.2913C=	XP_011514525.1:p.Phe971=
NM_000245.3:c.2856C=	NP_000236.2:p.Phe952=
NM_001127500.2:c.2910C=	NP_001120972.1:p.Phe970=
NM_001324402.1:c.1566C=	NP_001311331.1:p.Phe522=
XR_001744772.1:n.2987C=
NM_001127500.3:c.2910C=	NP_001120972.1:p.Phe970=
NM_000245.4:c.2856C= MANE Select	NP_000236.2:p.Phe952=
NM_001324402.2:c.1566C=	NP_001311331.1:p.Phe522=