Canonical Allele Identifier: CA1737037622

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771978C= , CM000669.2:g.116771978C=	GRCh38
NC_000007.13:g.116412032C= , CM000669.1:g.116412032C=	GRCh37
NC_000007.12:g.116199268C=	NCBI36
NG_008996.1:g.104574C= , LRG_662:g.104574C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*622C=	ENSP00000410980.2:n.*622C=
ENST00000318493.11:c.3071C=	ENSP00000317272.6:p.Thr1024=
ENST00000397752.8:c.3017C= MANE Select	ENSP00000380860.3:p.Thr1006=
ENST00000318493.10:c.3071C=	ENSP00000317272.6:p.Thr1024=
ENST00000397752.7:c.3017C=	ENSP00000380860.3:p.Thr1006=
ENST00000454623.1:c.283+324C=	ENSP00000398140.1:n.283+324C=
NM_000245.2:c.3017C=	NP_000236.2:p.Thr1006=
NM_001127500.1:c.3071C= , LRG_662t1:c.3071C=	NP_001120972.1:p.Thr1024=
XM_006715990.2:c.1727C=	XP_006716053.1:p.Thr576=
XM_006715991.2:c.1727C=	XP_006716054.1:p.Thr576=
XM_011516223.1:c.3074C=	XP_011514525.1:p.Thr1025=
NM_000245.3:c.3017C=	NP_000236.2:p.Thr1006=
NM_001127500.2:c.3071C=	NP_001120972.1:p.Thr1024=
NM_001324402.1:c.1727C=	NP_001311331.1:p.Thr576=
XR_001744772.1:n.3148C=
NM_001127500.3:c.3071C=	NP_001120972.1:p.Thr1024=
NM_000245.4:c.3017C= MANE Select	NP_000236.2:p.Thr1006=
NM_001324402.2:c.1727C=	NP_001311331.1:p.Thr576=