Canonical Allele Identifier: CA1737037567

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771852_116771853delinsTG , CM000669.2:g.116771852_116771853delinsTG	GRCh38
NC_000007.13:g.116411906_116411907delinsTG , CM000669.1:g.116411906_116411907delinsTG	GRCh37
NC_000007.12:g.116199142_116199143delinsTG	NCBI36
NG_008996.1:g.104448_104449delinsTG , LRG_662:g.104448_104449delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*496_*497delinsTG	ENSP00000410980.2:n.*496_*497delinsTG
ENST00000318493.11:c.2945_2946delinsTG	ENSP00000317272.6:p.Leu982=
ENST00000397752.8:c.2891_2892delinsTG MANE Select	ENSP00000380860.3:p.Leu964=
ENST00000318493.10:c.2945_2946delinsTG	ENSP00000317272.6:p.Leu982=
ENST00000397752.7:c.2891_2892delinsTG	ENSP00000380860.3:p.Leu964=
ENST00000454623.1:c.283+198_283+199delinsTG	ENSP00000398140.1:n.283+198_283+199delinsTG
NM_000245.2:c.2891_2892delinsTG	NP_000236.2:p.Leu964=
NM_001127500.1:c.2945_2946delinsTG , LRG_662t1:c.2945_2946delinsTG	NP_001120972.1:p.Leu982=
XM_006715990.2:c.1601_1602delinsTG	XP_006716053.1:p.Leu534=
XM_006715991.2:c.1601_1602delinsTG	XP_006716054.1:p.Leu534=
XM_011516223.1:c.2948_2949delinsTG	XP_011514525.1:p.Leu983=
NM_000245.3:c.2891_2892delinsTG	NP_000236.2:p.Leu964=
NM_001127500.2:c.2945_2946delinsTG	NP_001120972.1:p.Leu982=
NM_001324402.1:c.1601_1602delinsTG	NP_001311331.1:p.Leu534=
XR_001744772.1:n.3022_3023delinsTG
NM_001127500.3:c.2945_2946delinsTG	NP_001120972.1:p.Leu982=
NM_000245.4:c.2891_2892delinsTG MANE Select	NP_000236.2:p.Leu964=
NM_001324402.2:c.1601_1602delinsTG	NP_001311331.1:p.Leu534=