Canonical Allele Identifier: CA368977632

Gene: MET

Linked Data

• ClinVar Variation Id: 1970625
• ClinVar RCV Id: RCV002760449
• MyVariant Identifiers: chr7:g.116395422G>T (hg19) ; chr7:g.116755368G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116755368G>T , CM000669.2:g.116755368G>T	GRCh38
NC_000007.13:g.116395422G>T , CM000669.1:g.116395422G>T	GRCh37
NC_000007.12:g.116182658G>T	NCBI36
NG_008996.1:g.87964G>T , LRG_662:g.87964G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1715G>T	ENSP00000398776.2:p.Ser572Ile
ENST00000436117.3:c.1715G>T	ENSP00000410980.2:p.Ser572Ile
ENST00000318493.11:c.1715G>T	ENSP00000317272.6:p.Ser572Ile
ENST00000397752.8:c.1715G>T MANE Select	ENSP00000380860.3:p.Ser572Ile
ENST00000318493.10:c.1715G>T	ENSP00000317272.6:p.Ser572Ile
ENST00000397752.7:c.1715G>T	ENSP00000380860.3:p.Ser572Ile
ENST00000436117.2:c.1715G>T	ENSP00000410980.2:p.Ser572Ile
ENST00000495962.1:n.695G>T
NM_000245.2:c.1715G>T	NP_000236.2:p.Ser572Ile
NM_001127500.1:c.1715G>T , LRG_662t1:c.1715G>T	NP_001120972.1:p.Ser572Ile
XM_006715990.2:c.425G>T	XP_006716053.1:p.Ser142Ile
XM_006715991.2:c.425G>T	XP_006716054.1:p.Ser142Ile
XM_011516223.1:c.1772G>T	XP_011514525.1:p.Ser591Ile
NM_000245.3:c.1715G>T	NP_000236.2:p.Ser572Ile
NM_001127500.2:c.1715G>T	NP_001120972.1:p.Ser572Ile
NM_001324401.1:c.1715G>T	NP_001311330.1:p.Ser572Ile
NM_001324402.1:c.425G>T	NP_001311331.1:p.Ser142Ile
XR_001744772.1:n.1946G>T
NM_001127500.3:c.1715G>T	NP_001120972.1:p.Ser572Ile
NM_000245.4:c.1715G>T MANE Select	NP_000236.2:p.Ser572Ile
NM_001324401.2:c.1715G>T	NP_001311330.1:p.Ser572Ile
NM_001324402.2:c.425G>T	NP_001311331.1:p.Ser142Ile
NM_001324401.3:c.1715G>T	NP_001311330.1:p.Ser572Ile