Canonical Allele Identifier: CA1737014432
Gene: MET HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116783374T= , CM000669.2:g.116783374T= GRCh38
NC_000007.13:g.116423428T= , CM000669.1:g.116423428T= GRCh37
NC_000007.12:g.116210664T= NCBI36
NG_008996.1:g.115970T= , LRG_662:g.115970T=

Transcript Alleles

HGVS Amino-acid change
ENST00000436117.3:c.*1308T= ENSP00000410980.2:n.*1308T=
ENST00000318493.11:c.3757T= ENSP00000317272.6:p.Tyr1253=
ENST00000397752.8:c.3703T= MANE Select ENSP00000380860.3:p.Tyr1235=
ENST00000318493.10:c.3757T= ENSP00000317272.6:p.Tyr1253=
ENST00000397752.7:c.3703T= ENSP00000380860.3:p.Tyr1235=
NM_000245.2:c.3703T= NP_000236.2:p.Tyr1235=
NM_001127500.1:c.3757T= , LRG_662t1:c.3757T= NP_001120972.1:p.Tyr1253=
XM_006715990.2:c.2413T= XP_006716053.1:p.Tyr805=
XM_006715991.2:c.2413T= XP_006716054.1:p.Tyr805=
XM_011516223.1:c.3760T= XP_011514525.1:p.Tyr1254=
NM_000245.3:c.3703T= NP_000236.2:p.Tyr1235=
NM_001127500.2:c.3757T= NP_001120972.1:p.Tyr1253=
NM_001324402.1:c.2413T= NP_001311331.1:p.Tyr805=
XR_001744772.1:n.3834T=
NM_001127500.3:c.3757T= NP_001120972.1:p.Tyr1253=
NM_000245.4:c.3703T= MANE Select NP_000236.2:p.Tyr1235=
NM_001324402.2:c.2413T= NP_001311331.1:p.Tyr805=