Canonical Allele Identifier: CA368979437

Gene: MET

Linked Data

• ClinVar Variation Id: 1782924
• ClinVar RCV Id: RCV002410957
• dbSNP Id: rs763849125
• MyVariant Identifiers: chr7:g.116397561G>C (hg19) ; chr7:g.116757507G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116757507G>C , CM000669.2:g.116757507G>C	GRCh38
NC_000007.13:g.116397561G>C , CM000669.1:g.116397561G>C	GRCh37
NC_000007.12:g.116184797G>C	NCBI36
NG_008996.1:g.90103G>C , LRG_662:g.90103G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1933G>C	ENSP00000398776.2:p.Gly645Arg
ENST00000436117.3:c.1933G>C	ENSP00000410980.2:p.Gly645Arg
ENST00000318493.11:c.1933G>C	ENSP00000317272.6:p.Gly645Arg
ENST00000397752.8:c.1933G>C MANE Select	ENSP00000380860.3:p.Gly645Arg
ENST00000318493.10:c.1933G>C	ENSP00000317272.6:p.Gly645Arg
ENST00000397752.7:c.1933G>C	ENSP00000380860.3:p.Gly645Arg
ENST00000436117.2:c.1933G>C	ENSP00000410980.2:p.Gly645Arg
NM_000245.2:c.1933G>C	NP_000236.2:p.Gly645Arg
NM_001127500.1:c.1933G>C , LRG_662t1:c.1933G>C	NP_001120972.1:p.Gly645Arg
XM_006715990.2:c.643G>C	XP_006716053.1:p.Gly215Arg
XM_006715991.2:c.643G>C	XP_006716054.1:p.Gly215Arg
XM_011516223.1:c.1990G>C	XP_011514525.1:p.Gly664Arg
NM_000245.3:c.1933G>C	NP_000236.2:p.Gly645Arg
NM_001127500.2:c.1933G>C	NP_001120972.1:p.Gly645Arg
NM_001324401.1:c.1933G>C	NP_001311330.1:p.Gly645Arg
NM_001324402.1:c.643G>C	NP_001311331.1:p.Gly215Arg
XR_001744772.1:n.2164G>C
NM_001127500.3:c.1933G>C	NP_001120972.1:p.Gly645Arg
NM_000245.4:c.1933G>C MANE Select	NP_000236.2:p.Gly645Arg
NM_001324401.2:c.1933G>C	NP_001311330.1:p.Gly645Arg
NM_001324402.2:c.643G>C	NP_001311331.1:p.Gly215Arg
NM_001324401.3:c.1933G>C	NP_001311330.1:p.Gly645Arg