Canonical Allele Identifier: CA368968307

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116699168G>C , CM000669.2:g.116699168G>C	GRCh38
NC_000007.13:g.116339222G>C , CM000669.1:g.116339222G>C	GRCh37
NC_000007.12:g.116126458G>C	NCBI36
NG_008996.1:g.31764G>C , LRG_662:g.31764G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.84G>C MANE Select	NP_000236.2:p.Glu28Asp
ENST00000397752.8:c.84G>C MANE Select	ENSP00000380860.3:p.Glu28Asp
NM_000245.2:c.84G>C	NP_000236.2:p.Glu28Asp
NM_000245.3:c.84G>C	NP_000236.2:p.Glu28Asp
NM_001127500.1:c.84G>C , LRG_662t1:c.84G>C	NP_001120972.1:p.Glu28Asp
NM_001127500.2:c.84G>C	NP_001120972.1:p.Glu28Asp
NM_001127500.3:c.84G>C	NP_001120972.1:p.Glu28Asp
NM_001324401.1:c.84G>C	NP_001311330.1:p.Glu28Asp
NM_001324401.2:c.84G>C	NP_001311330.1:p.Glu28Asp
NM_001324401.3:c.84G>C	NP_001311330.1:p.Glu28Asp
NM_001324402.1:c.-91+26591G>C	NP_001311331.1:n.-91+26591G>C
NM_001324402.2:c.-91+26591G>C	NP_001311331.1:n.-91+26591G>C
ENST00000318493.10:c.84G>C	ENSP00000317272.6:p.Glu28Asp
ENST00000318493.11:c.84G>C	ENSP00000317272.6:p.Glu28Asp
ENST00000397752.7:c.84G>C	ENSP00000380860.3:p.Glu28Asp
ENST00000422097.2:c.84G>C	ENSP00000398776.2:p.Glu28Asp
ENST00000436117.2:c.84G>C	ENSP00000410980.2:p.Glu28Asp
ENST00000436117.3:c.84G>C	ENSP00000410980.2:p.Glu28Asp
ENST00000456159.1:c.141G>C	ENSP00000413857.1:p.Glu47Asp
XM_006715991.2:c.-91+26591G>C	XP_006716054.1:n.-91+26591G>C
XM_011516223.1:c.141G>C	XP_011514525.1:p.Glu47Asp
XR_001744772.1:n.315G>C