Canonical Allele Identifier: CA368986220

Gene: MET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771501A>T , CM000669.2:g.116771501A>T	GRCh38
NC_000007.13:g.116411555A>T , CM000669.1:g.116411555A>T	GRCh37
NC_000007.12:g.116198791A>T	NCBI36
NG_008996.1:g.104097A>T , LRG_662:g.104097A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*339A>T	ENSP00000410980.2:n.*339A>T
ENST00000318493.11:c.2788A>T	ENSP00000317272.6:p.Lys930Ter
ENST00000397752.8:c.2734A>T MANE Select	ENSP00000380860.3:p.Lys912Ter
ENST00000318493.10:c.2788A>T	ENSP00000317272.6:p.Lys930Ter
ENST00000397752.7:c.2734A>T	ENSP00000380860.3:p.Lys912Ter
ENST00000454623.1:c.130A>T	ENSP00000398140.1:p.Lys44Ter
NM_000245.2:c.2734A>T	NP_000236.2:p.Lys912Ter
NM_001127500.1:c.2788A>T , LRG_662t1:c.2788A>T	NP_001120972.1:p.Lys930Ter
XM_006715990.2:c.1444A>T	XP_006716053.1:p.Lys482Ter
XM_006715991.2:c.1444A>T	XP_006716054.1:p.Lys482Ter
XM_011516223.1:c.2791A>T	XP_011514525.1:p.Lys931Ter
NM_000245.3:c.2734A>T	NP_000236.2:p.Lys912Ter
NM_001127500.2:c.2788A>T	NP_001120972.1:p.Lys930Ter
NM_001324402.1:c.1444A>T	NP_001311331.1:p.Lys482Ter
XR_001744772.1:n.2865A>T
NM_001127500.3:c.2788A>T	NP_001120972.1:p.Lys930Ter
NM_000245.4:c.2734A>T MANE Select	NP_000236.2:p.Lys912Ter
NM_001324402.2:c.1444A>T	NP_001311331.1:p.Lys482Ter