Canonical Allele Identifier: CA2715296001

Gene: MET

Linked Data

• dbSNP Id: rs754953870

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116772040G>A , CM000669.2:g.116772040G>A	GRCh38
NC_000007.13:g.116412094G>A , CM000669.1:g.116412094G>A	GRCh37
NC_000007.12:g.116199330G>A	NCBI36
NG_008996.1:g.104636G>A , LRG_662:g.104636G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+51G>A	ENSP00000410980.2:n.*633+51G>A
ENST00000318493.11:c.3082+51G>A	ENSP00000317272.6:n.3082+51G>A
ENST00000397752.8:c.3028+51G>A MANE Select	ENSP00000380860.3:n.3028+51G>A
ENST00000318493.10:c.3082+51G>A	ENSP00000317272.6:n.3082+51G>A
ENST00000397752.7:c.3028+51G>A	ENSP00000380860.3:n.3028+51G>A
ENST00000454623.1:c.283+386G>A	ENSP00000398140.1:n.283+386G>A
NM_000245.2:c.3028+51G>A	NP_000236.2:n.3028+51G>A
NM_001127500.1:c.3082+51G>A , LRG_662t1:c.3082+51G>A	NP_001120972.1:n.3082+51G>A
XM_006715990.2:c.1738+51G>A	XP_006716053.1:n.1738+51G>A
XM_006715991.2:c.1738+51G>A	XP_006716054.1:n.1738+51G>A
XM_011516223.1:c.3085+51G>A	XP_011514525.1:n.3085+51G>A
NM_000245.3:c.3028+51G>A	NP_000236.2:n.3028+51G>A
NM_001127500.2:c.3082+51G>A	NP_001120972.1:n.3082+51G>A
NM_001324402.1:c.1738+51G>A	NP_001311331.1:n.1738+51G>A
XR_001744772.1:n.3159+51G>A
NM_001127500.3:c.3082+51G>A	NP_001120972.1:n.3082+51G>A
NM_000245.4:c.3028+51G>A MANE Select	NP_000236.2:n.3028+51G>A
NM_001324402.2:c.1738+51G>A	NP_001311331.1:n.1738+51G>A