Canonical Allele Identifier: CA832030405

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116797552G>C , CM000669.2:g.116797552G>C	GRCh38
NC_000007.13:g.116437606G>C , CM000669.1:g.116437606G>C	GRCh37
NC_000007.12:g.116224842G>C	NCBI36
NG_008996.1:g.130148G>C , LRG_662:g.130148G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*3206G>C	ENSP00000410980.2:n.*3206G>C
ENST00000318493.11:c.*1428G>C	ENSP00000317272.6:n.*1428G>C
ENST00000397752.8:c.*1428G>C MANE Select	ENSP00000380860.3:n.*1428G>C
ENST00000397752.7:c.*1428G>C	ENSP00000380860.3:n.*1428G>C
NM_000245.2:c.*1428G>C	NP_000236.2:n.*1428G>C
NM_001127500.1:c.*1428G>C , LRG_662t1:c.*1428G>C	NP_001120972.1:n.*1428G>C
XM_006715990.2:c.*1428G>C	XP_006716053.1:n.*1428G>C
XM_006715991.2:c.*1428G>C	XP_006716054.1:n.*1428G>C
XM_011516223.1:c.*1428G>C	XP_011514525.1:n.*1428G>C
NM_000245.3:c.*1428G>C	NP_000236.2:n.*1428G>C
NM_001127500.2:c.*1428G>C	NP_001120972.1:n.*1428G>C
NM_001324402.1:c.*1428G>C	NP_001311331.1:n.*1428G>C
XR_001744772.1:n.5732G>C
NM_001127500.3:c.*1428G>C	NP_001120972.1:n.*1428G>C
NM_000245.4:c.*1428G>C MANE Select	NP_000236.2:n.*1428G>C
NM_001324402.2:c.*1428G>C	NP_001311331.1:n.*1428G>C