Canonical Allele Identifier: CA2715553467

Gene: MET

Linked Data

• dbSNP Id: rs2116999387

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116772067T>A , CM000669.2:g.116772067T>A	GRCh38
NC_000007.13:g.116412121T>A , CM000669.1:g.116412121T>A	GRCh37
NC_000007.12:g.116199357T>A	NCBI36
NG_008996.1:g.104663T>A , LRG_662:g.104663T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+78T>A	ENSP00000410980.2:n.*633+78T>A
ENST00000318493.11:c.3082+78T>A	ENSP00000317272.6:n.3082+78T>A
ENST00000397752.8:c.3028+78T>A MANE Select	ENSP00000380860.3:n.3028+78T>A
ENST00000318493.10:c.3082+78T>A	ENSP00000317272.6:n.3082+78T>A
ENST00000397752.7:c.3028+78T>A	ENSP00000380860.3:n.3028+78T>A
ENST00000454623.1:c.283+413T>A	ENSP00000398140.1:n.283+413T>A
NM_000245.2:c.3028+78T>A	NP_000236.2:n.3028+78T>A
NM_001127500.1:c.3082+78T>A , LRG_662t1:c.3082+78T>A	NP_001120972.1:n.3082+78T>A
XM_006715990.2:c.1738+78T>A	XP_006716053.1:n.1738+78T>A
XM_006715991.2:c.1738+78T>A	XP_006716054.1:n.1738+78T>A
XM_011516223.1:c.3085+78T>A	XP_011514525.1:n.3085+78T>A
NM_000245.3:c.3028+78T>A	NP_000236.2:n.3028+78T>A
NM_001127500.2:c.3082+78T>A	NP_001120972.1:n.3082+78T>A
NM_001324402.1:c.1738+78T>A	NP_001311331.1:n.1738+78T>A
XR_001744772.1:n.3159+78T>A
NM_001127500.3:c.3082+78T>A	NP_001120972.1:n.3082+78T>A
NM_000245.4:c.3028+78T>A MANE Select	NP_000236.2:n.3028+78T>A
NM_001324402.2:c.1738+78T>A	NP_001311331.1:n.1738+78T>A