Canonical Allele Identifier: CA1737029669
Gene: MET HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000422097.2:c.2527C= ENSP00000398776.2:p.Pro843=
ENST00000436117.3:c.*132C= ENSP00000410980.2:n.*132C=
ENST00000318493.11:c.2581C= ENSP00000317272.6:p.Pro861=
ENST00000397752.8:c.2527C= MANE Select ENSP00000380860.3:p.Pro843=
ENST00000318493.10:c.2581C= ENSP00000317272.6:p.Pro861=
ENST00000397752.7:c.2527C= ENSP00000380860.3:p.Pro843=
ENST00000422097.1:c.367C= ENSP00000398776.1:p.Pro123=
NM_000245.2:c.2527C= NP_000236.2:p.Pro843=
NM_001127500.1:c.2581C= , LRG_662t1:c.2581C= NP_001120972.1:p.Pro861=
XM_006715990.2:c.1237C= XP_006716053.1:p.Pro413=
XM_006715991.2:c.1237C= XP_006716054.1:p.Pro413=
XM_011516223.1:c.2584C= XP_011514525.1:p.Pro862=
NM_000245.3:c.2527C= NP_000236.2:p.Pro843=
NM_001127500.2:c.2581C= NP_001120972.1:p.Pro861=
NM_001324401.1:c.2527C= NP_001311330.1:p.Pro843=
NM_001324402.1:c.1237C= NP_001311331.1:p.Pro413=
XR_001744772.1:n.2658C=
NM_001127500.3:c.2581C= NP_001120972.1:p.Pro861=
NM_000245.4:c.2527C= MANE Select NP_000236.2:p.Pro843=
NM_001324401.2:c.2527C= NP_001311330.1:p.Pro843=
NM_001324402.2:c.1237C= NP_001311331.1:p.Pro413=
NM_001324401.3:c.2527C= NP_001311330.1:p.Pro843=