Canonical Allele Identifier: CA368991695

Gene: MET

Linked Data

• dbSNP Id: rs2117066439
• MyVariant Identifiers: chr7:g.116423437C>A (hg19) ; chr7:g.116783383C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783383C>A , CM000669.2:g.116783383C>A	GRCh38
NC_000007.13:g.116423437C>A , CM000669.1:g.116423437C>A	GRCh37
NC_000007.12:g.116210673C>A	NCBI36
NG_008996.1:g.115979C>A , LRG_662:g.115979C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1317C>A	ENSP00000410980.2:n.*1317C>A
ENST00000318493.11:c.3766C>A	ENSP00000317272.6:p.His1256Asn
ENST00000397752.8:c.3712C>A MANE Select	ENSP00000380860.3:p.His1238Asn
ENST00000318493.10:c.3766C>A	ENSP00000317272.6:p.His1256Asn
ENST00000397752.7:c.3712C>A	ENSP00000380860.3:p.His1238Asn
NM_000245.2:c.3712C>A	NP_000236.2:p.His1238Asn
NM_001127500.1:c.3766C>A , LRG_662t1:c.3766C>A	NP_001120972.1:p.His1256Asn
XM_006715990.2:c.2422C>A	XP_006716053.1:p.His808Asn
XM_006715991.2:c.2422C>A	XP_006716054.1:p.His808Asn
XM_011516223.1:c.3769C>A	XP_011514525.1:p.His1257Asn
NM_000245.3:c.3712C>A	NP_000236.2:p.His1238Asn
NM_001127500.2:c.3766C>A	NP_001120972.1:p.His1256Asn
NM_001324402.1:c.2422C>A	NP_001311331.1:p.His808Asn
XR_001744772.1:n.3843C>A
NM_001127500.3:c.3766C>A	NP_001120972.1:p.His1256Asn
NM_000245.4:c.3712C>A MANE Select	NP_000236.2:p.His1238Asn
NM_001324402.2:c.2422C>A	NP_001311331.1:p.His808Asn