Canonical Allele Identifier: CA10623085

Gene: MET

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116798364G>A , CM000669.2:g.116798364G>A	GRCh38
NC_000007.13:g.116438418G>A , CM000669.1:g.116438418G>A	GRCh37
NC_000007.12:g.116225654G>A	NCBI36
NG_008996.1:g.130960G>A , LRG_662:g.130960G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*4018G>A	ENSP00000410980.2:n.*4018G>A
ENST00000318493.11:c.*2240G>A	ENSP00000317272.6:n.*2240G>A
ENST00000397752.8:c.*2240G>A MANE Select	ENSP00000380860.3:n.*2240G>A
ENST00000397752.7:c.*2240G>A	ENSP00000380860.3:n.*2240G>A
NM_000245.2:c.*2240G>A	NP_000236.2:n.*2240G>A
NM_001127500.1:c.*2240G>A , LRG_662t1:c.*2240G>A	NP_001120972.1:n.*2240G>A
XM_006715990.2:c.*2240G>A	XP_006716053.1:n.*2240G>A
XM_006715991.2:c.*2240G>A	XP_006716054.1:n.*2240G>A
XM_011516223.1:c.*2240G>A	XP_011514525.1:n.*2240G>A
NM_000245.3:c.*2240G>A	NP_000236.2:n.*2240G>A
NM_001127500.2:c.*2240G>A	NP_001120972.1:n.*2240G>A
NM_001324402.1:c.*2240G>A	NP_001311331.1:n.*2240G>A
XR_001744772.1:n.6544G>A
NM_001127500.3:c.*2240G>A	NP_001120972.1:n.*2240G>A
NM_000245.4:c.*2240G>A MANE Select	NP_000236.2:n.*2240G>A
NM_001324402.2:c.*2240G>A	NP_001311331.1:n.*2240G>A