Canonical Allele Identifier: CA2684591832
Gene: MET HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771398T>C , CM000669.2:g.116771398T>C GRCh38
NC_000007.13:g.116411452T>C , CM000669.1:g.116411452T>C GRCh37
NC_000007.12:g.116198688T>C NCBI36
NG_008996.1:g.103994T>C , LRG_662:g.103994T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*336-100T>C ENSP00000410980.2:n.*336-100T>C
ENST00000318493.11:c.2785-100T>C ENSP00000317272.6:n.2785-100T>C
ENST00000397752.8:c.2731-100T>C MANE Select ENSP00000380860.3:n.2731-100T>C
ENST00000318493.10:c.2785-100T>C ENSP00000317272.6:n.2785-100T>C
ENST00000397752.7:c.2731-100T>C ENSP00000380860.3:n.2731-100T>C
ENST00000454623.1:c.127-100T>C ENSP00000398140.1:n.127-100T>C
NM_000245.2:c.2731-100T>C NP_000236.2:n.2731-100T>C
NM_001127500.1:c.2785-100T>C , LRG_662t1:c.2785-100T>C NP_001120972.1:n.2785-100T>C
XM_006715990.2:c.1441-100T>C XP_006716053.1:n.1441-100T>C
XM_006715991.2:c.1441-100T>C XP_006716054.1:n.1441-100T>C
XM_011516223.1:c.2788-100T>C XP_011514525.1:n.2788-100T>C
NM_000245.3:c.2731-100T>C NP_000236.2:n.2731-100T>C
NM_001127500.2:c.2785-100T>C NP_001120972.1:n.2785-100T>C
NM_001324402.1:c.1441-100T>C NP_001311331.1:n.1441-100T>C
XR_001744772.1:n.2862-100T>C
NM_001127500.3:c.2785-100T>C NP_001120972.1:n.2785-100T>C
NM_000245.4:c.2731-100T>C MANE Select NP_000236.2:n.2731-100T>C
NM_001324402.2:c.1441-100T>C NP_001311331.1:n.1441-100T>C
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