Canonical Allele Identifier: CA164889217

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116700009A>C , CM000669.2:g.116700009A>C	GRCh38
NC_000007.13:g.116340063A>C , CM000669.1:g.116340063A>C	GRCh37
NC_000007.12:g.116127299A>C	NCBI36
NG_008996.1:g.32605A>C , LRG_662:g.32605A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.925A>C MANE Select	NP_000236.2:p.Thr309Pro
ENST00000397752.8:c.925A>C MANE Select	ENSP00000380860.3:p.Thr309Pro
NM_000245.2:c.925A>C	NP_000236.2:p.Thr309Pro
NM_000245.3:c.925A>C	NP_000236.2:p.Thr309Pro
NM_001127500.1:c.925A>C , LRG_662t1:c.925A>C	NP_001120972.1:p.Thr309Pro
NM_001127500.2:c.925A>C	NP_001120972.1:p.Thr309Pro
NM_001127500.3:c.925A>C	NP_001120972.1:p.Thr309Pro
NM_001324401.1:c.925A>C	NP_001311330.1:p.Thr309Pro
NM_001324401.2:c.925A>C	NP_001311330.1:p.Thr309Pro
NM_001324401.3:c.925A>C	NP_001311330.1:p.Thr309Pro
NM_001324402.1:c.-91+27432A>C	NP_001311331.1:n.-91+27432A>C
NM_001324402.2:c.-91+27432A>C	NP_001311331.1:n.-91+27432A>C
ENST00000318493.10:c.925A>C	ENSP00000317272.6:p.Thr309Pro
ENST00000318493.11:c.925A>C	ENSP00000317272.6:p.Thr309Pro
ENST00000397752.7:c.925A>C	ENSP00000380860.3:p.Thr309Pro
ENST00000422097.2:c.925A>C	ENSP00000398776.2:p.Thr309Pro
ENST00000436117.2:c.925A>C	ENSP00000410980.2:p.Thr309Pro
ENST00000436117.3:c.925A>C	ENSP00000410980.2:p.Thr309Pro
XM_006715991.2:c.-91+27432A>C	XP_006716054.1:n.-91+27432A>C
XM_011516223.1:c.982A>C	XP_011514525.1:p.Thr328Pro
XR_001744772.1:n.1156A>C