Canonical Allele Identifier: CA2580076299

Gene: MET

Linked Data

• ClinVar Variation Id: 2123743
• ClinVar RCV Id: RCV003035566

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783332_116783333delinsAT , CM000669.2:g.116783332_116783333delinsAT	GRCh38
NC_000007.13:g.116423386_116423387delinsAT , CM000669.1:g.116423386_116423387delinsAT	GRCh37
NC_000007.12:g.116210622_116210623delinsAT	NCBI36
NG_008996.1:g.115928_115929delinsAT , LRG_662:g.115928_115929delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1266_*1267delinsAT	ENSP00000410980.2:n.*1266_*1267delinsAT
ENST00000318493.11:c.3715_3716delinsAT	ENSP00000317272.6:p.Ala1239Ile
ENST00000397752.8:c.3661_3662delinsAT MANE Select	ENSP00000380860.3:p.Ala1221Ile
ENST00000318493.10:c.3715_3716delinsAT	ENSP00000317272.6:p.Ala1239Ile
ENST00000397752.7:c.3661_3662delinsAT	ENSP00000380860.3:p.Ala1221Ile
NM_000245.2:c.3661_3662delinsAT	NP_000236.2:p.Ala1221Ile
NM_001127500.1:c.3715_3716delinsAT , LRG_662t1:c.3715_3716delinsAT	NP_001120972.1:p.Ala1239Ile
XM_006715990.2:c.2371_2372delinsAT	XP_006716053.1:p.Ala791Ile
XM_006715991.2:c.2371_2372delinsAT	XP_006716054.1:p.Ala791Ile
XM_011516223.1:c.3718_3719delinsAT	XP_011514525.1:p.Ala1240Ile
NM_000245.3:c.3661_3662delinsAT	NP_000236.2:p.Ala1221Ile
NM_001127500.2:c.3715_3716delinsAT	NP_001120972.1:p.Ala1239Ile
NM_001324402.1:c.2371_2372delinsAT	NP_001311331.1:p.Ala791Ile
XR_001744772.1:n.3792_3793delinsAT
NM_001127500.3:c.3715_3716delinsAT	NP_001120972.1:p.Ala1239Ile
NM_000245.4:c.3661_3662delinsAT MANE Select	NP_000236.2:p.Ala1221Ile
NM_001324402.2:c.2371_2372delinsAT	NP_001311331.1:p.Ala791Ile