Canonical Allele Identifier: CA368982462

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116399522A>T (hg19) ; chr7:g.116759468A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759468A>T , CM000669.2:g.116759468A>T	GRCh38
NC_000007.13:g.116399522A>T , CM000669.1:g.116399522A>T	GRCh37
NC_000007.12:g.116186758A>T	NCBI36
NG_008996.1:g.92064A>T , LRG_662:g.92064A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2342A>T	ENSP00000398776.2:p.Glu781Val
ENST00000436117.3:c.2264+848A>T	ENSP00000410980.2:n.2264+848A>T
ENST00000318493.11:c.2396A>T	ENSP00000317272.6:p.Glu799Val
ENST00000397752.8:c.2342A>T MANE Select	ENSP00000380860.3:p.Glu781Val
ENST00000318493.10:c.2396A>T	ENSP00000317272.6:p.Glu799Val
ENST00000397752.7:c.2342A>T	ENSP00000380860.3:p.Glu781Val
ENST00000422097.1:c.182A>T	ENSP00000398776.1:p.Glu61Val
ENST00000436117.2:c.2264+848A>T	ENSP00000410980.2:n.2264+848A>T
NM_000245.2:c.2342A>T	NP_000236.2:p.Glu781Val
NM_001127500.1:c.2396A>T , LRG_662t1:c.2396A>T	NP_001120972.1:p.Glu799Val
XM_006715990.2:c.1052A>T	XP_006716053.1:p.Glu351Val
XM_006715991.2:c.1052A>T	XP_006716054.1:p.Glu351Val
XM_011516223.1:c.2399A>T	XP_011514525.1:p.Glu800Val
NM_000245.3:c.2342A>T	NP_000236.2:p.Glu781Val
NM_001127500.2:c.2396A>T	NP_001120972.1:p.Glu799Val
NM_001324401.1:c.2342A>T	NP_001311330.1:p.Glu781Val
NM_001324402.1:c.1052A>T	NP_001311331.1:p.Glu351Val
XR_001744772.1:n.2495+848A>T
NM_001127500.3:c.2396A>T	NP_001120972.1:p.Glu799Val
NM_000245.4:c.2342A>T MANE Select	NP_000236.2:p.Glu781Val
NM_001324401.2:c.2342A>T	NP_001311330.1:p.Glu781Val
NM_001324402.2:c.1052A>T	NP_001311331.1:p.Glu351Val
NM_001324401.3:c.2342A>T	NP_001311330.1:p.Glu781Val