Canonical Allele Identifier: CA16612159

Gene: MET

Linked Data

• ClinVar Variation Id: 411880
• ClinVar RCV Id: RCV002230190 ; RCV002451133
• dbSNP Id: rs905891313
• gnomAD v3: 7-116763212-C-G
• gnomAD v4: 7-116763212-C-G
• MyVariant Identifiers: chr7:g.116403266C>G (hg19) ; chr7:g.116763212C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763212C>G , CM000669.2:g.116763212C>G	GRCh38
NC_000007.13:g.116403266C>G , CM000669.1:g.116403266C>G	GRCh37
NC_000007.12:g.116190502C>G	NCBI36
NG_008996.1:g.95808C>G , LRG_662:g.95808C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2527C>G	ENSP00000398776.2:p.Pro843Ala
ENST00000436117.3:c.*132C>G	ENSP00000410980.2:n.*132C>G
ENST00000318493.11:c.2581C>G	ENSP00000317272.6:p.Pro861Ala
ENST00000397752.8:c.2527C>G MANE Select	ENSP00000380860.3:p.Pro843Ala
ENST00000318493.10:c.2581C>G	ENSP00000317272.6:p.Pro861Ala
ENST00000397752.7:c.2527C>G	ENSP00000380860.3:p.Pro843Ala
ENST00000422097.1:c.367C>G	ENSP00000398776.1:p.Pro123Ala
NM_000245.2:c.2527C>G	NP_000236.2:p.Pro843Ala
NM_001127500.1:c.2581C>G , LRG_662t1:c.2581C>G	NP_001120972.1:p.Pro861Ala
XM_006715990.2:c.1237C>G	XP_006716053.1:p.Pro413Ala
XM_006715991.2:c.1237C>G	XP_006716054.1:p.Pro413Ala
XM_011516223.1:c.2584C>G	XP_011514525.1:p.Pro862Ala
NM_000245.3:c.2527C>G	NP_000236.2:p.Pro843Ala
NM_001127500.2:c.2581C>G	NP_001120972.1:p.Pro861Ala
NM_001324401.1:c.2527C>G	NP_001311330.1:p.Pro843Ala
NM_001324402.1:c.1237C>G	NP_001311331.1:p.Pro413Ala
XR_001744772.1:n.2658C>G
NM_001127500.3:c.2581C>G	NP_001120972.1:p.Pro861Ala
NM_000245.4:c.2527C>G MANE Select	NP_000236.2:p.Pro843Ala
NM_001324401.2:c.2527C>G	NP_001311330.1:p.Pro843Ala
NM_001324402.2:c.1237C>G	NP_001311331.1:p.Pro413Ala
NM_001324401.3:c.2527C>G	NP_001311330.1:p.Pro843Ala