Canonical Allele Identifier: CA1737037737

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116772232_116772233delinsCA , CM000669.2:g.116772232_116772233delinsCA	GRCh38
NC_000007.13:g.116412286_116412287delinsCA , CM000669.1:g.116412286_116412287delinsCA	GRCh37
NC_000007.12:g.116199522_116199523delinsCA	NCBI36
NG_008996.1:g.104828_104829delinsCA , LRG_662:g.104828_104829delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*633+243_*633+244delinsCA	ENSP00000410980.2:n.*633+243_*633+244delinsCA
ENST00000318493.11:c.3082+243_3082+244delinsCA	ENSP00000317272.6:n.3082+243_3082+244delinsCA
ENST00000397752.8:c.3028+243_3028+244delinsCA MANE Select	ENSP00000380860.3:n.3028+243_3028+244delinsCA
ENST00000318493.10:c.3082+243_3082+244delinsCA	ENSP00000317272.6:n.3082+243_3082+244delinsCA
ENST00000397752.7:c.3028+243_3028+244delinsCA	ENSP00000380860.3:n.3028+243_3028+244delinsCA
ENST00000454623.1:c.283+578_283+579delinsCA	ENSP00000398140.1:n.283+578_283+579delinsCA
NM_000245.2:c.3028+243_3028+244delinsCA	NP_000236.2:n.3028+243_3028+244delinsCA
NM_001127500.1:c.3082+243_3082+244delinsCA , LRG_662t1:c.3082+243_3082+244delinsCA	NP_001120972.1:n.3082+243_3082+244delinsCA
XM_006715990.2:c.1738+243_1738+244delinsCA	XP_006716053.1:n.1738+243_1738+244delinsCA
XM_006715991.2:c.1738+243_1738+244delinsCA	XP_006716054.1:n.1738+243_1738+244delinsCA
XM_011516223.1:c.3085+243_3085+244delinsCA	XP_011514525.1:n.3085+243_3085+244delinsCA
NM_000245.3:c.3028+243_3028+244delinsCA	NP_000236.2:n.3028+243_3028+244delinsCA
NM_001127500.2:c.3082+243_3082+244delinsCA	NP_001120972.1:n.3082+243_3082+244delinsCA
NM_001324402.1:c.1738+243_1738+244delinsCA	NP_001311331.1:n.1738+243_1738+244delinsCA
XR_001744772.1:n.3159+243_3159+244delinsCA
NM_001127500.3:c.3082+243_3082+244delinsCA	NP_001120972.1:n.3082+243_3082+244delinsCA
NM_000245.4:c.3028+243_3028+244delinsCA MANE Select	NP_000236.2:n.3028+243_3028+244delinsCA
NM_001324402.2:c.1738+243_1738+244delinsCA	NP_001311331.1:n.1738+243_1738+244delinsCA