Canonical Allele Identifier: CA164886457
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs38850
gnomAD v2: 7-116337649-G-A
gnomAD v3: 7-116697595-G-A
gnomAD v4: 7-116697595-G-A
MyVariant Identifiers: chr7:g.116337649G>A (hg19) chr7:g.116697595G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116697595G>A , CM000669.2:g.116697595G>A GRCh38
NC_000007.13:g.116337649G>A , CM000669.1:g.116337649G>A GRCh37
NC_000007.12:g.116124885G>A NCBI36
NG_008996.1:g.30191G>A , LRG_662:g.30191G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000422097.2:c.-14-1476G>A ENSP00000398776.2:n.-14-1476G>A
ENST00000436117.3:c.-14-1476G>A ENSP00000410980.2:n.-14-1476G>A
ENST00000318493.11:c.-14-1476G>A ENSP00000317272.6:n.-14-1476G>A
ENST00000397752.8:c.-14-1476G>A MANE Select ENSP00000380860.3:n.-14-1476G>A
ENST00000318493.10:c.-14-1476G>A ENSP00000317272.6:n.-14-1476G>A
ENST00000397752.7:c.-14-1476G>A ENSP00000380860.3:n.-14-1476G>A
ENST00000456159.1:c.44-1476G>A ENSP00000413857.1:n.44-1476G>A
NM_000245.2:c.-14-1476G>A NP_000236.2:n.-14-1476G>A
NM_001127500.1:c.-14-1476G>A , LRG_662t1:c.-14-1476G>A NP_001120972.1:n.-14-1476G>A
XM_006715991.2:c.-91+25018G>A XP_006716054.1:n.-91+25018G>A
XM_011516223.1:c.44-1476G>A XP_011514525.1:n.44-1476G>A
NM_000245.3:c.-14-1476G>A NP_000236.2:n.-14-1476G>A
NM_001127500.2:c.-14-1476G>A NP_001120972.1:n.-14-1476G>A
NM_001324401.1:c.-14-1476G>A NP_001311330.1:n.-14-1476G>A
NM_001324402.1:c.-91+25018G>A NP_001311331.1:n.-91+25018G>A
XR_001744772.1:n.218-1476G>A
NM_001127500.3:c.-14-1476G>A NP_001120972.1:n.-14-1476G>A
NM_000245.4:c.-14-1476G>A MANE Select NP_000236.2:n.-14-1476G>A
NM_001324401.2:c.-14-1476G>A NP_001311330.1:n.-14-1476G>A
NM_001324402.2:c.-91+25018G>A NP_001311331.1:n.-91+25018G>A
NM_001324401.3:c.-14-1476G>A NP_001311330.1:n.-14-1476G>A
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