Canonical Allele Identifier: CA1737024832
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116759099C= , CM000669.2:g.116759099C= GRCh38
NC_000007.13:g.116399153C= , CM000669.1:g.116399153C= GRCh37
NC_000007.12:g.116186389C= NCBI36
NG_008996.1:g.91695C= , LRG_662:g.91695C=

Transcript Alleles

HGVS Amino-acid change
ENST00000422097.2:c.2265-292C= ENSP00000398776.2:n.2265-292C=
ENST00000436117.3:c.2264+479C= ENSP00000410980.2:n.2264+479C=
ENST00000318493.11:c.2265-238C= ENSP00000317272.6:n.2265-238C=
ENST00000397752.8:c.2265-292C= MANE Select ENSP00000380860.3:n.2265-292C=
ENST00000318493.10:c.2265-238C= ENSP00000317272.6:n.2265-238C=
ENST00000397752.7:c.2265-292C= ENSP00000380860.3:n.2265-292C=
ENST00000422097.1:c.105-292C= ENSP00000398776.1:n.105-292C=
ENST00000436117.2:c.2264+479C= ENSP00000410980.2:n.2264+479C=
NM_000245.2:c.2265-292C= NP_000236.2:n.2265-292C=
NM_001127500.1:c.2265-238C= , LRG_662t1:c.2265-238C= NP_001120972.1:n.2265-238C=
XM_006715990.2:c.975-292C= XP_006716053.1:n.975-292C=
XM_006715991.2:c.975-292C= XP_006716054.1:n.975-292C=
XM_011516223.1:c.2322-292C= XP_011514525.1:n.2322-292C=
NM_000245.3:c.2265-292C= NP_000236.2:n.2265-292C=
NM_001127500.2:c.2265-238C= NP_001120972.1:n.2265-238C=
NM_001324401.1:c.2265-292C= NP_001311330.1:n.2265-292C=
NM_001324402.1:c.975-292C= NP_001311331.1:n.975-292C=
XR_001744772.1:n.2495+479C=
NM_001127500.3:c.2265-238C= NP_001120972.1:n.2265-238C=
NM_000245.4:c.2265-292C= MANE Select NP_000236.2:n.2265-292C=
NM_001324401.2:c.2265-292C= NP_001311330.1:n.2265-292C=
NM_001324402.2:c.975-292C= NP_001311331.1:n.975-292C=
NM_001324401.3:c.2265-292C= NP_001311330.1:n.2265-292C=