Canonical Allele Identifier: CA368968296

Gene: MET

Linked Data

• ClinVar Variation Id: 1442248
• ClinVar RCV Id: RCV001952945
• dbSNP Id: rs2116579656
• MyVariant Identifiers: chr7:g.116339217A>T (hg19) ; chr7:g.116699163A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116699163A>T , CM000669.2:g.116699163A>T	GRCh38
NC_000007.13:g.116339217A>T , CM000669.1:g.116339217A>T	GRCh37
NC_000007.12:g.116126453A>T	NCBI36
NG_008996.1:g.31759A>T , LRG_662:g.31759A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.79A>T	ENSP00000398776.2:p.Lys27Ter
ENST00000436117.3:c.79A>T	ENSP00000410980.2:p.Lys27Ter
ENST00000318493.11:c.79A>T	ENSP00000317272.6:p.Lys27Ter
ENST00000397752.8:c.79A>T MANE Select	ENSP00000380860.3:p.Lys27Ter
ENST00000318493.10:c.79A>T	ENSP00000317272.6:p.Lys27Ter
ENST00000397752.7:c.79A>T	ENSP00000380860.3:p.Lys27Ter
ENST00000436117.2:c.79A>T	ENSP00000410980.2:p.Lys27Ter
ENST00000456159.1:c.136A>T	ENSP00000413857.1:p.Lys46Ter
NM_000245.2:c.79A>T	NP_000236.2:p.Lys27Ter
NM_001127500.1:c.79A>T , LRG_662t1:c.79A>T	NP_001120972.1:p.Lys27Ter
XM_006715991.2:c.-91+26586A>T	XP_006716054.1:n.-91+26586A>T
XM_011516223.1:c.136A>T	XP_011514525.1:p.Lys46Ter
NM_000245.3:c.79A>T	NP_000236.2:p.Lys27Ter
NM_001127500.2:c.79A>T	NP_001120972.1:p.Lys27Ter
NM_001324401.1:c.79A>T	NP_001311330.1:p.Lys27Ter
NM_001324402.1:c.-91+26586A>T	NP_001311331.1:n.-91+26586A>T
XR_001744772.1:n.310A>T
NM_001127500.3:c.79A>T	NP_001120972.1:p.Lys27Ter
NM_000245.4:c.79A>T MANE Select	NP_000236.2:p.Lys27Ter
NM_001324401.2:c.79A>T	NP_001311330.1:p.Lys27Ter
NM_001324402.2:c.-91+26586A>T	NP_001311331.1:n.-91+26586A>T
NM_001324401.3:c.79A>T	NP_001311330.1:p.Lys27Ter