Canonical Allele Identifier: CA368987216

Gene: MET

Linked Data

• ClinVar Variation Id: 822593
• ClinVar RCV Id: RCV001018063
• dbSNP Id: rs910937816
• MyVariant Identifiers: chr7:g.116411975G>C (hg19) ; chr7:g.116771921G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771921G>C , CM000669.2:g.116771921G>C	GRCh38
NC_000007.13:g.116411975G>C , CM000669.1:g.116411975G>C	GRCh37
NC_000007.12:g.116199211G>C	NCBI36
NG_008996.1:g.104517G>C , LRG_662:g.104517G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*565G>C	ENSP00000410980.2:n.*565G>C
ENST00000318493.11:c.3014G>C	ENSP00000317272.6:p.Arg1005Pro
ENST00000397752.8:c.2960G>C MANE Select	ENSP00000380860.3:p.Arg987Pro
ENST00000318493.10:c.3014G>C	ENSP00000317272.6:p.Arg1005Pro
ENST00000397752.7:c.2960G>C	ENSP00000380860.3:p.Arg987Pro
ENST00000454623.1:c.283+267G>C	ENSP00000398140.1:n.283+267G>C
NM_000245.2:c.2960G>C	NP_000236.2:p.Arg987Pro
NM_001127500.1:c.3014G>C , LRG_662t1:c.3014G>C	NP_001120972.1:p.Arg1005Pro
XM_006715990.2:c.1670G>C	XP_006716053.1:p.Arg557Pro
XM_006715991.2:c.1670G>C	XP_006716054.1:p.Arg557Pro
XM_011516223.1:c.3017G>C	XP_011514525.1:p.Arg1006Pro
NM_000245.3:c.2960G>C	NP_000236.2:p.Arg987Pro
NM_001127500.2:c.3014G>C	NP_001120972.1:p.Arg1005Pro
NM_001324402.1:c.1670G>C	NP_001311331.1:p.Arg557Pro
XR_001744772.1:n.3091G>C
NM_001127500.3:c.3014G>C	NP_001120972.1:p.Arg1005Pro
NM_000245.4:c.2960G>C MANE Select	NP_000236.2:p.Arg987Pro
NM_001324402.2:c.1670G>C	NP_001311331.1:p.Arg557Pro