Canonical Allele Identifier: CA12637773
Gene: MET HGNC NCBI

Linked Data

ClinVar Variation Id: 1183625
ClinVar RCV Id: RCV001541506
dbSNP Id: rs10215153
gnomAD v2: 7-116399131-G-A
gnomAD v3: 7-116759077-G-A
gnomAD v4: 7-116759077-G-A
MyVariant Identifiers: chr7:g.116399131G>A (hg19) chr7:g.116759077G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116759077G>A , CM000669.2:g.116759077G>A GRCh38
NC_000007.13:g.116399131G>A , CM000669.1:g.116399131G>A GRCh37
NC_000007.12:g.116186367G>A NCBI36
NG_008996.1:g.91673G>A , LRG_662:g.91673G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000422097.2:c.2265-314G>A ENSP00000398776.2:n.2265-314G>A
ENST00000436117.3:c.2264+457G>A ENSP00000410980.2:n.2264+457G>A
ENST00000318493.11:c.2265-260G>A ENSP00000317272.6:n.2265-260G>A
ENST00000397752.8:c.2265-314G>A MANE Select ENSP00000380860.3:n.2265-314G>A
ENST00000318493.10:c.2265-260G>A ENSP00000317272.6:n.2265-260G>A
ENST00000397752.7:c.2265-314G>A ENSP00000380860.3:n.2265-314G>A
ENST00000422097.1:c.105-314G>A ENSP00000398776.1:n.105-314G>A
ENST00000436117.2:c.2264+457G>A ENSP00000410980.2:n.2264+457G>A
NM_000245.2:c.2265-314G>A NP_000236.2:n.2265-314G>A
NM_001127500.1:c.2265-260G>A , LRG_662t1:c.2265-260G>A NP_001120972.1:n.2265-260G>A
XM_006715990.2:c.975-314G>A XP_006716053.1:n.975-314G>A
XM_006715991.2:c.975-314G>A XP_006716054.1:n.975-314G>A
XM_011516223.1:c.2322-314G>A XP_011514525.1:n.2322-314G>A
NM_000245.3:c.2265-314G>A NP_000236.2:n.2265-314G>A
NM_001127500.2:c.2265-260G>A NP_001120972.1:n.2265-260G>A
NM_001324401.1:c.2265-314G>A NP_001311330.1:n.2265-314G>A
NM_001324402.1:c.975-314G>A NP_001311331.1:n.975-314G>A
XR_001744772.1:n.2495+457G>A
NM_001127500.3:c.2265-260G>A NP_001120972.1:n.2265-260G>A
NM_000245.4:c.2265-314G>A MANE Select NP_000236.2:n.2265-314G>A
NM_001324401.2:c.2265-314G>A NP_001311330.1:n.2265-314G>A
NM_001324402.2:c.975-314G>A NP_001311331.1:n.975-314G>A
NM_001324401.3:c.2265-314G>A NP_001311330.1:n.2265-314G>A
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