Canonical Allele Identifier: CA368982505

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116399528G>T (hg19) ; chr7:g.116759474G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759474G>T , CM000669.2:g.116759474G>T	GRCh38
NC_000007.13:g.116399528G>T , CM000669.1:g.116399528G>T	GRCh37
NC_000007.12:g.116186764G>T	NCBI36
NG_008996.1:g.92070G>T , LRG_662:g.92070G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2348G>T	ENSP00000398776.2:p.Gly783Val
ENST00000436117.3:c.2264+854G>T	ENSP00000410980.2:n.2264+854G>T
ENST00000318493.11:c.2402G>T	ENSP00000317272.6:p.Gly801Val
ENST00000397752.8:c.2348G>T MANE Select	ENSP00000380860.3:p.Gly783Val
ENST00000318493.10:c.2402G>T	ENSP00000317272.6:p.Gly801Val
ENST00000397752.7:c.2348G>T	ENSP00000380860.3:p.Gly783Val
ENST00000422097.1:c.188G>T	ENSP00000398776.1:p.Gly63Val
ENST00000436117.2:c.2264+854G>T	ENSP00000410980.2:n.2264+854G>T
NM_000245.2:c.2348G>T	NP_000236.2:p.Gly783Val
NM_001127500.1:c.2402G>T , LRG_662t1:c.2402G>T	NP_001120972.1:p.Gly801Val
XM_006715990.2:c.1058G>T	XP_006716053.1:p.Gly353Val
XM_006715991.2:c.1058G>T	XP_006716054.1:p.Gly353Val
XM_011516223.1:c.2405G>T	XP_011514525.1:p.Gly802Val
NM_000245.3:c.2348G>T	NP_000236.2:p.Gly783Val
NM_001127500.2:c.2402G>T	NP_001120972.1:p.Gly801Val
NM_001324401.1:c.2348G>T	NP_001311330.1:p.Gly783Val
NM_001324402.1:c.1058G>T	NP_001311331.1:p.Gly353Val
XR_001744772.1:n.2495+854G>T
NM_001127500.3:c.2402G>T	NP_001120972.1:p.Gly801Val
NM_000245.4:c.2348G>T MANE Select	NP_000236.2:p.Gly783Val
NM_001324401.2:c.2348G>T	NP_001311330.1:p.Gly783Val
NM_001324402.2:c.1058G>T	NP_001311331.1:p.Gly353Val
NM_001324401.3:c.2348G>T	NP_001311330.1:p.Gly783Val