Canonical Allele Identifier: CA368983557

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116403272G>T (hg19) ; chr7:g.116763218G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763218G>T , CM000669.2:g.116763218G>T	GRCh38
NC_000007.13:g.116403272G>T , CM000669.1:g.116403272G>T	GRCh37
NC_000007.12:g.116190508G>T	NCBI36
NG_008996.1:g.95814G>T , LRG_662:g.95814G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2533G>T	ENSP00000398776.2:p.Glu845Ter
ENST00000436117.3:c.*138G>T	ENSP00000410980.2:n.*138G>T
ENST00000318493.11:c.2587G>T	ENSP00000317272.6:p.Glu863Ter
ENST00000397752.8:c.2533G>T MANE Select	ENSP00000380860.3:p.Glu845Ter
ENST00000318493.10:c.2587G>T	ENSP00000317272.6:p.Glu863Ter
ENST00000397752.7:c.2533G>T	ENSP00000380860.3:p.Glu845Ter
ENST00000422097.1:c.373G>T	ENSP00000398776.1:p.Glu125Ter
NM_000245.2:c.2533G>T	NP_000236.2:p.Glu845Ter
NM_001127500.1:c.2587G>T , LRG_662t1:c.2587G>T	NP_001120972.1:p.Glu863Ter
XM_006715990.2:c.1243G>T	XP_006716053.1:p.Glu415Ter
XM_006715991.2:c.1243G>T	XP_006716054.1:p.Glu415Ter
XM_011516223.1:c.2590G>T	XP_011514525.1:p.Glu864Ter
NM_000245.3:c.2533G>T	NP_000236.2:p.Glu845Ter
NM_001127500.2:c.2587G>T	NP_001120972.1:p.Glu863Ter
NM_001324401.1:c.2533G>T	NP_001311330.1:p.Glu845Ter
NM_001324402.1:c.1243G>T	NP_001311331.1:p.Glu415Ter
XR_001744772.1:n.2664G>T
NM_001127500.3:c.2587G>T	NP_001120972.1:p.Glu863Ter
NM_000245.4:c.2533G>T MANE Select	NP_000236.2:p.Glu845Ter
NM_001324401.2:c.2533G>T	NP_001311330.1:p.Glu845Ter
NM_001324402.2:c.1243G>T	NP_001311331.1:p.Glu415Ter
NM_001324401.3:c.2533G>T	NP_001311330.1:p.Glu845Ter