Canonical Allele Identifier: CA160413

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771869C>T , CM000669.2:g.116771869C>T	GRCh38
NC_000007.13:g.116411923C>T , CM000669.1:g.116411923C>T	GRCh37
NC_000007.12:g.116199159C>T	NCBI36
NG_008996.1:g.104465C>T , LRG_662:g.104465C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.2908C>T MANE Select	NP_000236.2:p.Arg970Cys
ENST00000397752.8:c.2908C>T MANE Select	ENSP00000380860.3:p.Arg970Cys
NM_000245.2:c.2908C>T	NP_000236.2:p.Arg970Cys
NM_000245.3:c.2908C>T	NP_000236.2:p.Arg970Cys
NM_001127500.1:c.2962C>T , LRG_662t1:c.2962C>T	NP_001120972.1:p.Arg988Cys
NM_001127500.2:c.2962C>T	NP_001120972.1:p.Arg988Cys
NM_001127500.3:c.2962C>T	NP_001120972.1:p.Arg988Cys
NM_001324402.1:c.1618C>T	NP_001311331.1:p.Arg540Cys
NM_001324402.2:c.1618C>T	NP_001311331.1:p.Arg540Cys
ENST00000318493.10:c.2962C>T	ENSP00000317272.6:p.Arg988Cys
ENST00000318493.11:c.2962C>T	ENSP00000317272.6:p.Arg988Cys
ENST00000397752.7:c.2908C>T	ENSP00000380860.3:p.Arg970Cys
ENST00000436117.3:c.*513C>T	ENSP00000410980.2:n.*513C>T
ENST00000454623.1:c.283+215C>T	ENSP00000398140.1:n.283+215C>T
XM_006715990.2:c.1618C>T	XP_006716053.1:p.Arg540Cys
XM_006715991.2:c.1618C>T	XP_006716054.1:p.Arg540Cys
XM_011516223.1:c.2965C>T	XP_011514525.1:p.Arg989Cys
XR_001744772.1:n.3039C>T