Canonical Allele Identifier: CA1737037599

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771925T= , CM000669.2:g.116771925T=	GRCh38
NC_000007.13:g.116411979T= , CM000669.1:g.116411979T=	GRCh37
NC_000007.12:g.116199215T=	NCBI36
NG_008996.1:g.104521T= , LRG_662:g.104521T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*569T=	ENSP00000410980.2:n.*569T=
ENST00000318493.11:c.3018T=	ENSP00000317272.6:p.Ser1006=
ENST00000397752.8:c.2964T= MANE Select	ENSP00000380860.3:p.Ser988=
ENST00000318493.10:c.3018T=	ENSP00000317272.6:p.Ser1006=
ENST00000397752.7:c.2964T=	ENSP00000380860.3:p.Ser988=
ENST00000454623.1:c.283+271T=	ENSP00000398140.1:n.283+271T=
NM_000245.2:c.2964T=	NP_000236.2:p.Ser988=
NM_001127500.1:c.3018T= , LRG_662t1:c.3018T=	NP_001120972.1:p.Ser1006=
XM_006715990.2:c.1674T=	XP_006716053.1:p.Ser558=
XM_006715991.2:c.1674T=	XP_006716054.1:p.Ser558=
XM_011516223.1:c.3021T=	XP_011514525.1:p.Ser1007=
NM_000245.3:c.2964T=	NP_000236.2:p.Ser988=
NM_001127500.2:c.3018T=	NP_001120972.1:p.Ser1006=
NM_001324402.1:c.1674T=	NP_001311331.1:p.Ser558=
XR_001744772.1:n.3095T=
NM_001127500.3:c.3018T=	NP_001120972.1:p.Ser1006=
NM_000245.4:c.2964T= MANE Select	NP_000236.2:p.Ser988=
NM_001324402.2:c.1674T=	NP_001311331.1:p.Ser558=