Canonical Allele Identifier: CA1737012337

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116782048C= , CM000669.2:g.116782048C=	GRCh38
NC_000007.13:g.116422102C= , CM000669.1:g.116422102C=	GRCh37
NC_000007.12:g.116209338C=	NCBI36
NG_008996.1:g.114644C= , LRG_662:g.114644C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1188C=	ENSP00000410980.2:n.*1188C=
ENST00000318493.11:c.3637C=	ENSP00000317272.6:p.Leu1213=
ENST00000397752.8:c.3583C= MANE Select	ENSP00000380860.3:p.Leu1195=
ENST00000318493.10:c.3637C=	ENSP00000317272.6:p.Leu1213=
ENST00000397752.7:c.3583C=	ENSP00000380860.3:p.Leu1195=
NM_000245.2:c.3583C=	NP_000236.2:p.Leu1195=
NM_001127500.1:c.3637C= , LRG_662t1:c.3637C=	NP_001120972.1:p.Leu1213=
XM_006715990.2:c.2293C=	XP_006716053.1:p.Leu765=
XM_006715991.2:c.2293C=	XP_006716054.1:p.Leu765=
XM_011516223.1:c.3640C=	XP_011514525.1:p.Leu1214=
NM_000245.3:c.3583C=	NP_000236.2:p.Leu1195=
NM_001127500.2:c.3637C=	NP_001120972.1:p.Leu1213=
NM_001324402.1:c.2293C=	NP_001311331.1:p.Leu765=
XR_001744772.1:n.3714C=
NM_001127500.3:c.3637C=	NP_001120972.1:p.Leu1213=
NM_000245.4:c.3583C= MANE Select	NP_000236.2:p.Leu1195=
NM_001324402.2:c.2293C=	NP_001311331.1:p.Leu765=