Canonical Allele Identifier: CA164894222

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116758474T>C , CM000669.2:g.116758474T>C	GRCh38
NC_000007.13:g.116398528T>C , CM000669.1:g.116398528T>C	GRCh37
NC_000007.12:g.116185764T>C	NCBI36
NG_008996.1:g.91070T>C , LRG_662:g.91070T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.2118T>C MANE Select	NP_000236.2:p.Ile706=
ENST00000397752.8:c.2118T>C MANE Select	ENSP00000380860.3:p.Ile706=
NM_000245.2:c.2118T>C	NP_000236.2:p.Ile706=
NM_000245.3:c.2118T>C	NP_000236.2:p.Ile706=
NM_001127500.1:c.2118T>C , LRG_662t1:c.2118T>C	NP_001120972.1:p.Ile706=
NM_001127500.2:c.2118T>C	NP_001120972.1:p.Ile706=
NM_001127500.3:c.2118T>C	NP_001120972.1:p.Ile706=
NM_001324401.1:c.2118T>C	NP_001311330.1:p.Ile706=
NM_001324401.2:c.2118T>C	NP_001311330.1:p.Ile706=
NM_001324401.3:c.2118T>C	NP_001311330.1:p.Ile706=
NM_001324402.1:c.828T>C	NP_001311331.1:p.Ile276=
NM_001324402.2:c.828T>C	NP_001311331.1:p.Ile276=
ENST00000318493.10:c.2118T>C	ENSP00000317272.6:p.Ile706=
ENST00000318493.11:c.2118T>C	ENSP00000317272.6:p.Ile706=
ENST00000397752.7:c.2118T>C	ENSP00000380860.3:p.Ile706=
ENST00000422097.2:c.2118T>C	ENSP00000398776.2:p.Ile706=
ENST00000436117.2:c.2118T>C	ENSP00000410980.2:p.Ile706=
ENST00000436117.3:c.2118T>C	ENSP00000410980.2:p.Ile706=
XM_006715990.2:c.828T>C	XP_006716053.1:p.Ile276=
XM_006715991.2:c.828T>C	XP_006716054.1:p.Ile276=
XM_011516223.1:c.2175T>C	XP_011514525.1:p.Ile725=
XR_001744772.1:n.2349T>C