Canonical Allele Identifier: CA2715553228

Gene: MET

Linked Data

• dbSNP Id: rs2116995292

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771820_116771821delinsGG , CM000669.2:g.116771820_116771821delinsGG	GRCh38
NC_000007.13:g.116411874_116411875delinsGG , CM000669.1:g.116411874_116411875delinsGG	GRCh37
NC_000007.12:g.116199110_116199111delinsGG	NCBI36
NG_008996.1:g.104416_104417delinsGG , LRG_662:g.104416_104417delinsGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-29_*493-28delinsGG	ENSP00000410980.2:n.*493-29_*493-28delinsGG
ENST00000318493.11:c.2942-29_2942-28delinsGG	ENSP00000317272.6:n.2942-29_2942-28delinsGG
ENST00000397752.8:c.2888-29_2888-28delinsGG MANE Select	ENSP00000380860.3:n.2888-29_2888-28delinsGG
ENST00000318493.10:c.2942-29_2942-28delinsGG	ENSP00000317272.6:n.2942-29_2942-28delinsGG
ENST00000397752.7:c.2888-29_2888-28delinsGG	ENSP00000380860.3:n.2888-29_2888-28delinsGG
ENST00000454623.1:c.283+166_283+167delinsGG	ENSP00000398140.1:n.283+166_283+167delinsGG
NM_000245.2:c.2888-29_2888-28delinsGG	NP_000236.2:n.2888-29_2888-28delinsGG
NM_001127500.1:c.2942-29_2942-28delinsGG , LRG_662t1:c.2942-29_2942-28delinsGG	NP_001120972.1:n.2942-29_2942-28delinsGG
XM_006715990.2:c.1598-29_1598-28delinsGG	XP_006716053.1:n.1598-29_1598-28delinsGG
XM_006715991.2:c.1598-29_1598-28delinsGG	XP_006716054.1:n.1598-29_1598-28delinsGG
XM_011516223.1:c.2945-29_2945-28delinsGG	XP_011514525.1:n.2945-29_2945-28delinsGG
NM_000245.3:c.2888-29_2888-28delinsGG	NP_000236.2:n.2888-29_2888-28delinsGG
NM_001127500.2:c.2942-29_2942-28delinsGG	NP_001120972.1:n.2942-29_2942-28delinsGG
NM_001324402.1:c.1598-29_1598-28delinsGG	NP_001311331.1:n.1598-29_1598-28delinsGG
XR_001744772.1:n.3019-29_3019-28delinsGG
NM_001127500.3:c.2942-29_2942-28delinsGG	NP_001120972.1:n.2942-29_2942-28delinsGG
NM_000245.4:c.2888-29_2888-28delinsGG MANE Select	NP_000236.2:n.2888-29_2888-28delinsGG
NM_001324402.2:c.1598-29_1598-28delinsGG	NP_001311331.1:n.1598-29_1598-28delinsGG