Canonical Allele Identifier: CA457447559

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116411959A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771905A>C , CM000669.2:g.116771905A>C	GRCh38
NC_000007.13:g.116411959A>C , CM000669.1:g.116411959A>C	GRCh37
NC_000007.12:g.116199195A>C	NCBI36
NG_008996.1:g.104501A>C , LRG_662:g.104501A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*549A>C	ENSP00000410980.2:n.*549A>C
ENST00000318493.11:c.2998A>C	ENSP00000317272.6:p.Arg1000=
ENST00000397752.8:c.2944A>C MANE Select	ENSP00000380860.3:p.Arg982=
ENST00000318493.10:c.2998A>C	ENSP00000317272.6:p.Arg1000=
ENST00000397752.7:c.2944A>C	ENSP00000380860.3:p.Arg982=
ENST00000454623.1:c.283+251A>C	ENSP00000398140.1:n.283+251A>C
NM_000245.2:c.2944A>C	NP_000236.2:p.Arg982=
NM_001127500.1:c.2998A>C , LRG_662t1:c.2998A>C	NP_001120972.1:p.Arg1000=
XM_006715990.2:c.1654A>C	XP_006716053.1:p.Arg552=
XM_006715991.2:c.1654A>C	XP_006716054.1:p.Arg552=
XM_011516223.1:c.3001A>C	XP_011514525.1:p.Arg1001=
NM_000245.3:c.2944A>C	NP_000236.2:p.Arg982=
NM_001127500.2:c.2998A>C	NP_001120972.1:p.Arg1000=
NM_001324402.1:c.1654A>C	NP_001311331.1:p.Arg552=
XR_001744772.1:n.3075A>C
NM_001127500.3:c.2998A>C	NP_001120972.1:p.Arg1000=
NM_000245.4:c.2944A>C MANE Select	NP_000236.2:p.Arg982=
NM_001324402.2:c.1654A>C	NP_001311331.1:p.Arg552=