Canonical Allele Identifier: CA368987225
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1798868
ClinVar RCV Id: RCV002435839
dbSNP Id: rs1794848550

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771924G>A , CM000669.2:g.116771924G>A GRCh38
NC_000007.13:g.116411978G>A , CM000669.1:g.116411978G>A GRCh37
NC_000007.12:g.116199214G>A NCBI36
NG_008996.1:g.104520G>A , LRG_662:g.104520G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*568G>A ENSP00000410980.2:n.*568G>A
ENST00000318493.11:c.3017G>A ENSP00000317272.6:p.Ser1006Asn
ENST00000397752.8:c.2963G>A MANE Select ENSP00000380860.3:p.Ser988Asn
ENST00000318493.10:c.3017G>A ENSP00000317272.6:p.Ser1006Asn
ENST00000397752.7:c.2963G>A ENSP00000380860.3:p.Ser988Asn
ENST00000454623.1:c.283+270G>A ENSP00000398140.1:n.283+270G>A
NM_000245.2:c.2963G>A NP_000236.2:p.Ser988Asn
NM_001127500.1:c.3017G>A , LRG_662t1:c.3017G>A NP_001120972.1:p.Ser1006Asn
XM_006715990.2:c.1673G>A XP_006716053.1:p.Ser558Asn
XM_006715991.2:c.1673G>A XP_006716054.1:p.Ser558Asn
XM_011516223.1:c.3020G>A XP_011514525.1:p.Ser1007Asn
NM_000245.3:c.2963G>A NP_000236.2:p.Ser988Asn
NM_001127500.2:c.3017G>A NP_001120972.1:p.Ser1006Asn
NM_001324402.1:c.1673G>A NP_001311331.1:p.Ser558Asn
XR_001744772.1:n.3094G>A
NM_001127500.3:c.3017G>A NP_001120972.1:p.Ser1006Asn
NM_000245.4:c.2963G>A MANE Select NP_000236.2:p.Ser988Asn
NM_001324402.2:c.1673G>A NP_001311331.1:p.Ser558Asn