Canonical Allele Identifier: CA1737041217
Community Standard Title: NM_000245.4(MET):c.*1987C=
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116798111C= , CM000669.2:g.116798111C= GRCh38
NC_000007.13:g.116438165C= , CM000669.1:g.116438165C= GRCh37
NC_000007.12:g.116225401C= NCBI36
NG_008996.1:g.130707C= , LRG_662:g.130707C=

Transcript Alleles

HGVS Amino-acid Change
NM_000245.4:c.*1987C= MANE Select NP_000236.2:n.*1987C=
ENST00000397752.8:c.*1987C= MANE Select ENSP00000380860.3:n.*1987C=
NM_000245.2:c.*1987C= NP_000236.2:n.*1987C=
NM_000245.3:c.*1987C= NP_000236.2:n.*1987C=
NM_001127500.1:c.*1987C= , LRG_662t1:c.*1987C= NP_001120972.1:n.*1987C=
NM_001127500.2:c.*1987C= NP_001120972.1:n.*1987C=
NM_001127500.3:c.*1987C= NP_001120972.1:n.*1987C=
NM_001324402.1:c.*1987C= NP_001311331.1:n.*1987C=
NM_001324402.2:c.*1987C= NP_001311331.1:n.*1987C=
ENST00000318493.11:c.*1987C= ENSP00000317272.6:n.*1987C=
ENST00000397752.7:c.*1987C= ENSP00000380860.3:n.*1987C=
ENST00000436117.3:c.*3765C= ENSP00000410980.2:n.*3765C=
XM_006715990.2:c.*1987C= XP_006716053.1:n.*1987C=
XM_006715991.2:c.*1987C= XP_006716054.1:n.*1987C=
XM_011516223.1:c.*1987C= XP_011514525.1:n.*1987C=
XR_001744772.1:n.6291C=