Canonical Allele Identifier: CA1737037450

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771632G= , CM000669.2:g.116771632G=	GRCh38
NC_000007.13:g.116411686G= , CM000669.1:g.116411686G=	GRCh37
NC_000007.12:g.116198922G=	NCBI36
NG_008996.1:g.104228G= , LRG_662:g.104228G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*470G=	ENSP00000410980.2:n.*470G=
ENST00000318493.11:c.2919G=	ENSP00000317272.6:p.Leu973=
ENST00000397752.8:c.2865G= MANE Select	ENSP00000380860.3:p.Leu955=
ENST00000318493.10:c.2919G=	ENSP00000317272.6:p.Leu973=
ENST00000397752.7:c.2865G=	ENSP00000380860.3:p.Leu955=
ENST00000454623.1:c.261G=	ENSP00000398140.1:p.Leu87=
NM_000245.2:c.2865G=	NP_000236.2:p.Leu955=
NM_001127500.1:c.2919G= , LRG_662t1:c.2919G=	NP_001120972.1:p.Leu973=
XM_006715990.2:c.1575G=	XP_006716053.1:p.Leu525=
XM_006715991.2:c.1575G=	XP_006716054.1:p.Leu525=
XM_011516223.1:c.2922G=	XP_011514525.1:p.Leu974=
NM_000245.3:c.2865G=	NP_000236.2:p.Leu955=
NM_001127500.2:c.2919G=	NP_001120972.1:p.Leu973=
NM_001324402.1:c.1575G=	NP_001311331.1:p.Leu525=
XR_001744772.1:n.2996G=
NM_001127500.3:c.2919G=	NP_001120972.1:p.Leu973=
NM_000245.4:c.2865G= MANE Select	NP_000236.2:p.Leu955=
NM_001324402.2:c.1575G=	NP_001311331.1:p.Leu525=