Canonical Allele Identifier: CA2580617369

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771850_116771881del , CM000669.2:g.116771850_116771881del	GRCh38
NC_000007.13:g.116411904_116411935del , CM000669.1:g.116411904_116411935del	GRCh37
NC_000007.12:g.116199140_116199171del	NCBI36
NG_008996.1:g.104446_104477del , LRG_662:g.104446_104477del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*494_*525del	ENSP00000410980.2:n.*494_*525del
ENST00000318493.11:c.2943_2974del	ENSP00000317272.6:p.Asp981GlufsTer9
ENST00000397752.8:c.2889_2920del MANE Select	ENSP00000380860.3:p.Asp963GlufsTer9
ENST00000318493.10:c.2943_2974del	ENSP00000317272.6:p.Asp981GlufsTer9
ENST00000397752.7:c.2889_2920del	ENSP00000380860.3:p.Asp963GlufsTer9
ENST00000454623.1:c.283+196_283+227del	ENSP00000398140.1:n.283+196_283+227del
NM_000245.2:c.2889_2920del	NP_000236.2:p.Asp963GlufsTer9
NM_001127500.1:c.2943_2974del , LRG_662t1:c.2943_2974del	NP_001120972.1:p.Asp981GlufsTer9
XM_006715990.2:c.1599_1630del	XP_006716053.1:p.Asp533GlufsTer9
XM_006715991.2:c.1599_1630del	XP_006716054.1:p.Asp533GlufsTer9
XM_011516223.1:c.2946_2977del	XP_011514525.1:p.Asp982GlufsTer9
NM_000245.3:c.2889_2920del	NP_000236.2:p.Asp963GlufsTer9
NM_001127500.2:c.2943_2974del	NP_001120972.1:p.Asp981GlufsTer9
NM_001324402.1:c.1599_1630del	NP_001311331.1:p.Asp533GlufsTer9
XR_001744772.1:n.3020_3051del
NM_001127500.3:c.2943_2974del	NP_001120972.1:p.Asp981GlufsTer9
NM_000245.4:c.2889_2920del MANE Select	NP_000236.2:p.Asp963GlufsTer9
NM_001324402.2:c.1599_1630del	NP_001311331.1:p.Asp533GlufsTer9