Canonical Allele Identifier: CA368968129

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116699082A>C , CM000669.2:g.116699082A>C	GRCh38
NC_000007.13:g.116339136A>C , CM000669.1:g.116339136A>C	GRCh37
NC_000007.12:g.116126372A>C	NCBI36
NG_008996.1:g.31678A>C , LRG_662:g.31678A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.-3A>C	ENSP00000398776.2:n.-3A>C
ENST00000436117.3:c.-3A>C	ENSP00000410980.2:n.-3A>C
ENST00000318493.11:c.-3A>C	ENSP00000317272.6:n.-3A>C
ENST00000397752.8:c.-3A>C MANE Select	ENSP00000380860.3:n.-3A>C
ENST00000318493.10:c.-3A>C	ENSP00000317272.6:n.-3A>C
ENST00000397752.7:c.-3A>C	ENSP00000380860.3:n.-3A>C
ENST00000456159.1:c.55A>C	ENSP00000413857.1:p.Ile19Leu
NM_000245.2:c.-3A>C	NP_000236.2:n.-3A>C
NM_001127500.1:c.-3A>C , LRG_662t1:c.-3A>C	NP_001120972.1:n.-3A>C
XM_006715991.2:c.-91+26505A>C	XP_006716054.1:n.-91+26505A>C
XM_011516223.1:c.55A>C	XP_011514525.1:p.Ile19Leu
NM_000245.3:c.-3A>C	NP_000236.2:n.-3A>C
NM_001127500.2:c.-3A>C	NP_001120972.1:n.-3A>C
NM_001324401.1:c.-3A>C	NP_001311330.1:n.-3A>C
NM_001324402.1:c.-91+26505A>C	NP_001311331.1:n.-91+26505A>C
XR_001744772.1:n.229A>C
NM_001127500.3:c.-3A>C	NP_001120972.1:n.-3A>C
NM_000245.4:c.-3A>C MANE Select	NP_000236.2:n.-3A>C
NM_001324401.2:c.-3A>C	NP_001311330.1:n.-3A>C
NM_001324402.2:c.-91+26505A>C	NP_001311331.1:n.-91+26505A>C
NM_001324401.3:c.-3A>C	NP_001311330.1:n.-3A>C