Canonical Allele Identifier: CA368986215

Gene: MET

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771499G>C , CM000669.2:g.116771499G>C	GRCh38
NC_000007.13:g.116411553G>C , CM000669.1:g.116411553G>C	GRCh37
NC_000007.12:g.116198789G>C	NCBI36
NG_008996.1:g.104095G>C , LRG_662:g.104095G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*337G>C	ENSP00000410980.2:n.*337G>C
ENST00000318493.11:c.2786G>C	ENSP00000317272.6:p.Trp929Ser
ENST00000397752.8:c.2732G>C MANE Select	ENSP00000380860.3:p.Trp911Ser
ENST00000318493.10:c.2786G>C	ENSP00000317272.6:p.Trp929Ser
ENST00000397752.7:c.2732G>C	ENSP00000380860.3:p.Trp911Ser
ENST00000454623.1:c.128G>C	ENSP00000398140.1:p.Trp43Ser
NM_000245.2:c.2732G>C	NP_000236.2:p.Trp911Ser
NM_001127500.1:c.2786G>C , LRG_662t1:c.2786G>C	NP_001120972.1:p.Trp929Ser
XM_006715990.2:c.1442G>C	XP_006716053.1:p.Trp481Ser
XM_006715991.2:c.1442G>C	XP_006716054.1:p.Trp481Ser
XM_011516223.1:c.2789G>C	XP_011514525.1:p.Trp930Ser
NM_000245.3:c.2732G>C	NP_000236.2:p.Trp911Ser
NM_001127500.2:c.2786G>C	NP_001120972.1:p.Trp929Ser
NM_001324402.1:c.1442G>C	NP_001311331.1:p.Trp481Ser
XR_001744772.1:n.2863G>C
NM_001127500.3:c.2786G>C	NP_001120972.1:p.Trp929Ser
NM_000245.4:c.2732G>C MANE Select	NP_000236.2:p.Trp911Ser
NM_001324402.2:c.1442G>C	NP_001311331.1:p.Trp481Ser