Canonical Allele Identifier: CA1737037688

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116772110C= , CM000669.2:g.116772110C=	GRCh38
NC_000007.13:g.116412164C= , CM000669.1:g.116412164C=	GRCh37
NC_000007.12:g.116199400C=	NCBI36
NG_008996.1:g.104706C= , LRG_662:g.104706C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+121C=	ENSP00000410980.2:n.*633+121C=
ENST00000318493.11:c.3082+121C=	ENSP00000317272.6:n.3082+121C=
ENST00000397752.8:c.3028+121C= MANE Select	ENSP00000380860.3:n.3028+121C=
ENST00000318493.10:c.3082+121C=	ENSP00000317272.6:n.3082+121C=
ENST00000397752.7:c.3028+121C=	ENSP00000380860.3:n.3028+121C=
ENST00000454623.1:c.283+456C=	ENSP00000398140.1:n.283+456C=
NM_000245.2:c.3028+121C=	NP_000236.2:n.3028+121C=
NM_001127500.1:c.3082+121C= , LRG_662t1:c.3082+121C=	NP_001120972.1:n.3082+121C=
XM_006715990.2:c.1738+121C=	XP_006716053.1:n.1738+121C=
XM_006715991.2:c.1738+121C=	XP_006716054.1:n.1738+121C=
XM_011516223.1:c.3085+121C=	XP_011514525.1:n.3085+121C=
NM_000245.3:c.3028+121C=	NP_000236.2:n.3028+121C=
NM_001127500.2:c.3082+121C=	NP_001120972.1:n.3082+121C=
NM_001324402.1:c.1738+121C=	NP_001311331.1:n.1738+121C=
XR_001744772.1:n.3159+121C=
NM_001127500.3:c.3082+121C=	NP_001120972.1:n.3082+121C=
NM_000245.4:c.3028+121C= MANE Select	NP_000236.2:n.3028+121C=
NM_001324402.2:c.1738+121C=	NP_001311331.1:n.1738+121C=