Canonical Allele Identifier: CA1736993243

Gene: MET COMETT

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116681748A= , CM000669.2:g.116681748A=	GRCh38
NC_000007.13:g.116321802A= , CM000669.1:g.116321802A=	GRCh37
NC_000007.12:g.116109038A=	NCBI36
NG_008996.1:g.14344A= , LRG_662:g.14344A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000245.4:c.-15+9171A= (MET) MANE Select	NP_000236.2:n.-15+9171A=
ENST00000397752.8:c.-15+9171A= (MET) MANE Select	ENSP00000380860.3:n.-15+9171A=
NM_000245.2:c.-15+9171A= (MET)	NP_000236.2:n.-15+9171A=
NM_000245.3:c.-15+9171A= (MET)	NP_000236.2:n.-15+9171A=
NM_001127500.1:c.-15+9171A= , LRG_662t1:c.-15+9171A= (MET)	NP_001120972.1:n.-15+9171A=
NM_001127500.2:c.-15+9171A= (MET)	NP_001120972.1:n.-15+9171A=
NM_001127500.3:c.-15+9171A= (MET)	NP_001120972.1:n.-15+9171A=
NM_001324401.1:c.-15+9171A= (MET)	NP_001311330.1:n.-15+9171A=
NM_001324401.2:c.-15+9171A= (MET)	NP_001311330.1:n.-15+9171A=
NM_001324401.3:c.-15+9171A= (MET)	NP_001311330.1:n.-15+9171A=
NM_001324402.1:c.-91+9171A= (MET)	NP_001311331.1:n.-91+9171A=
NM_001324402.2:c.-91+9171A= (MET)	NP_001311331.1:n.-91+9171A=
NR_165032.1:n.87+6193T= (COMETT)
NR_165033.1:n.87+6193T= (COMETT)
ENST00000318493.10:c.-15+9171A= (MET)	ENSP00000317272.6:n.-15+9171A=
ENST00000318493.11:c.-15+9171A= (MET)	ENSP00000317272.6:n.-15+9171A=
ENST00000397752.7:c.-15+9171A= (MET)	ENSP00000380860.3:n.-15+9171A=
ENST00000422097.2:c.-15+9171A= (MET)	ENSP00000398776.2:n.-15+9171A=
ENST00000436117.3:c.-15+9171A= (MET)	ENSP00000410980.2:n.-15+9171A=
ENST00000456159.1:c.-8+9171A= (MET)	ENSP00000413857.1:n.-8+9171A=
XM_006715991.2:c.-91+9171A= (MET)	XP_006716054.1:n.-91+9171A=
XM_011516223.1:c.-8+9171A= (MET)	XP_011514525.1:n.-8+9171A=
XR_001744772.1:n.167+9171A= (MET)