Canonical Allele Identifier: CA1737037586

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771896C= , CM000669.2:g.116771896C=	GRCh38
NC_000007.13:g.116411950C= , CM000669.1:g.116411950C=	GRCh37
NC_000007.12:g.116199186C=	NCBI36
NG_008996.1:g.104492C= , LRG_662:g.104492C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*540C=	ENSP00000410980.2:n.*540C=
ENST00000318493.11:c.2989C=	ENSP00000317272.6:p.His997=
ENST00000397752.8:c.2935C= MANE Select	ENSP00000380860.3:p.His979=
ENST00000318493.10:c.2989C=	ENSP00000317272.6:p.His997=
ENST00000397752.7:c.2935C=	ENSP00000380860.3:p.His979=
ENST00000454623.1:c.283+242C=	ENSP00000398140.1:n.283+242C=
NM_000245.2:c.2935C=	NP_000236.2:p.His979=
NM_001127500.1:c.2989C= , LRG_662t1:c.2989C=	NP_001120972.1:p.His997=
XM_006715990.2:c.1645C=	XP_006716053.1:p.His549=
XM_006715991.2:c.1645C=	XP_006716054.1:p.His549=
XM_011516223.1:c.2992C=	XP_011514525.1:p.His998=
NM_000245.3:c.2935C=	NP_000236.2:p.His979=
NM_001127500.2:c.2989C=	NP_001120972.1:p.His997=
NM_001324402.1:c.1645C=	NP_001311331.1:p.His549=
XR_001744772.1:n.3066C=
NM_001127500.3:c.2989C=	NP_001120972.1:p.His997=
NM_000245.4:c.2935C= MANE Select	NP_000236.2:p.His979=
NM_001324402.2:c.1645C=	NP_001311331.1:p.His549=