Canonical Allele Identifier: CA4448549

Gene: MET

Linked Data - Expert Curation

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116769745C>T , CM000669.2:g.116769745C>T	GRCh38
NC_000007.13:g.116409799C>T , CM000669.1:g.116409799C>T	GRCh37
NC_000007.12:g.116197035C>T	NCBI36
NG_008996.1:g.102341C>T , LRG_662:g.102341C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2684C>T	ENSP00000398776.2:p.Thr895Met
ENST00000436117.3:c.*289C>T	ENSP00000410980.2:n.*289C>T
ENST00000318493.11:c.2738C>T	ENSP00000317272.6:p.Thr913Met
ENST00000397752.8:c.2684C>T MANE Select	ENSP00000380860.3:p.Thr895Met
ENST00000318493.10:c.2738C>T	ENSP00000317272.6:p.Thr913Met
ENST00000397752.7:c.2684C>T	ENSP00000380860.3:p.Thr895Met
ENST00000422097.1:c.524C>T	ENSP00000398776.1:p.Thr175Met
ENST00000454623.1:c.80C>T	ENSP00000398140.1:p.Thr27Met
NM_000245.2:c.2684C>T	NP_000236.2:p.Thr895Met
NM_001127500.1:c.2738C>T , LRG_662t1:c.2738C>T	NP_001120972.1:p.Thr913Met
XM_006715990.2:c.1394C>T	XP_006716053.1:p.Thr465Met
XM_006715991.2:c.1394C>T	XP_006716054.1:p.Thr465Met
XM_011516223.1:c.2741C>T	XP_011514525.1:p.Thr914Met
NM_000245.3:c.2684C>T	NP_000236.2:p.Thr895Met
NM_001127500.2:c.2738C>T	NP_001120972.1:p.Thr913Met
NM_001324401.1:c.2684C>T	NP_001311330.1:p.Thr895Met
NM_001324402.1:c.1394C>T	NP_001311331.1:p.Thr465Met
XR_001744772.1:n.2815C>T
NM_001127500.3:c.2738C>T	NP_001120972.1:p.Thr913Met
NM_000245.4:c.2684C>T MANE Select	NP_000236.2:p.Thr895Met
NM_001324401.2:c.2684C>T	NP_001311330.1:p.Thr895Met
NM_001324402.2:c.1394C>T	NP_001311331.1:p.Thr465Met
NM_001324401.3:c.2684C>T	NP_001311330.1:p.Thr895Met