Canonical Allele Identifier: CA4448765

Gene: MET

Linked Data

• ClinVar Variation Id: 1129771
• ClinVar RCV Id: RCV001463032 ; RCV002350941 ; RCV003900594
• dbSNP Id: rs201747580
• ExAC: 7:116423427 C / T
• gnomAD v2: 7-116423427-C-T
• gnomAD v3: 7-116783373-C-T
• gnomAD v4: 7-116783373-C-T
• MyVariant Identifiers: chr7:g.116423427C>T (hg19) ; chr7:g.116783373C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783373C>T , CM000669.2:g.116783373C>T	GRCh38
NC_000007.13:g.116423427C>T , CM000669.1:g.116423427C>T	GRCh37
NC_000007.12:g.116210663C>T	NCBI36
NG_008996.1:g.115969C>T , LRG_662:g.115969C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1307C>T	ENSP00000410980.2:n.*1307C>T
ENST00000318493.11:c.3756C>T	ENSP00000317272.6:p.Tyr1252=
ENST00000397752.8:c.3702C>T MANE Select	ENSP00000380860.3:p.Tyr1234=
ENST00000318493.10:c.3756C>T	ENSP00000317272.6:p.Tyr1252=
ENST00000397752.7:c.3702C>T	ENSP00000380860.3:p.Tyr1234=
NM_000245.2:c.3702C>T	NP_000236.2:p.Tyr1234=
NM_001127500.1:c.3756C>T , LRG_662t1:c.3756C>T	NP_001120972.1:p.Tyr1252=
XM_006715990.2:c.2412C>T	XP_006716053.1:p.Tyr804=
XM_006715991.2:c.2412C>T	XP_006716054.1:p.Tyr804=
XM_011516223.1:c.3759C>T	XP_011514525.1:p.Tyr1253=
NM_000245.3:c.3702C>T	NP_000236.2:p.Tyr1234=
NM_001127500.2:c.3756C>T	NP_001120972.1:p.Tyr1252=
NM_001324402.1:c.2412C>T	NP_001311331.1:p.Tyr804=
XR_001744772.1:n.3833C>T
NM_001127500.3:c.3756C>T	NP_001120972.1:p.Tyr1252=
NM_000245.4:c.3702C>T MANE Select	NP_000236.2:p.Tyr1234=
NM_001324402.2:c.2412C>T	NP_001311331.1:p.Tyr804=