Canonical Allele Identifier: CA1737037533

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771800G= , CM000669.2:g.116771800G=	GRCh38
NC_000007.13:g.116411854G= , CM000669.1:g.116411854G=	GRCh37
NC_000007.12:g.116199090G=	NCBI36
NG_008996.1:g.104396G= , LRG_662:g.104396G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-49G=	ENSP00000410980.2:n.*493-49G=
ENST00000318493.11:c.2942-49G=	ENSP00000317272.6:n.2942-49G=
ENST00000397752.8:c.2888-49G= MANE Select	ENSP00000380860.3:n.2888-49G=
ENST00000318493.10:c.2942-49G=	ENSP00000317272.6:n.2942-49G=
ENST00000397752.7:c.2888-49G=	ENSP00000380860.3:n.2888-49G=
ENST00000454623.1:c.283+146G=	ENSP00000398140.1:n.283+146G=
NM_000245.2:c.2888-49G=	NP_000236.2:n.2888-49G=
NM_001127500.1:c.2942-49G= , LRG_662t1:c.2942-49G=	NP_001120972.1:n.2942-49G=
XM_006715990.2:c.1598-49G=	XP_006716053.1:n.1598-49G=
XM_006715991.2:c.1598-49G=	XP_006716054.1:n.1598-49G=
XM_011516223.1:c.2945-49G=	XP_011514525.1:n.2945-49G=
NM_000245.3:c.2888-49G=	NP_000236.2:n.2888-49G=
NM_001127500.2:c.2942-49G=	NP_001120972.1:n.2942-49G=
NM_001324402.1:c.1598-49G=	NP_001311331.1:n.1598-49G=
XR_001744772.1:n.3019-49G=
NM_001127500.3:c.2942-49G=	NP_001120972.1:n.2942-49G=
NM_000245.4:c.2888-49G= MANE Select	NP_000236.2:n.2888-49G=
NM_001324402.2:c.1598-49G=	NP_001311331.1:n.1598-49G=