Canonical Allele Identifier: CA1737025450

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759455_116759456delinsAT , CM000669.2:g.116759455_116759456delinsAT	GRCh38
NC_000007.13:g.116399509_116399510delinsAT , CM000669.1:g.116399509_116399510delinsAT	GRCh37
NC_000007.12:g.116186745_116186746delinsAT	NCBI36
NG_008996.1:g.92051_92052delinsAT , LRG_662:g.92051_92052delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2329_2330delinsAT	ENSP00000398776.2:p.Ile777=
ENST00000436117.3:c.2264+835_2264+836delinsAT	ENSP00000410980.2:n.2264+835_2264+836delinsAT
ENST00000318493.11:c.2383_2384delinsAT	ENSP00000317272.6:p.Ile795=
ENST00000397752.8:c.2329_2330delinsAT MANE Select	ENSP00000380860.3:p.Ile777=
ENST00000318493.10:c.2383_2384delinsAT	ENSP00000317272.6:p.Ile795=
ENST00000397752.7:c.2329_2330delinsAT	ENSP00000380860.3:p.Ile777=
ENST00000422097.1:c.169_170delinsAT	ENSP00000398776.1:p.Ile57=
ENST00000436117.2:c.2264+835_2264+836delinsAT	ENSP00000410980.2:n.2264+835_2264+836delinsAT
NM_000245.2:c.2329_2330delinsAT	NP_000236.2:p.Ile777=
NM_001127500.1:c.2383_2384delinsAT , LRG_662t1:c.2383_2384delinsAT	NP_001120972.1:p.Ile795=
XM_006715990.2:c.1039_1040delinsAT	XP_006716053.1:p.Ile347=
XM_006715991.2:c.1039_1040delinsAT	XP_006716054.1:p.Ile347=
XM_011516223.1:c.2386_2387delinsAT	XP_011514525.1:p.Ile796=
NM_000245.3:c.2329_2330delinsAT	NP_000236.2:p.Ile777=
NM_001127500.2:c.2383_2384delinsAT	NP_001120972.1:p.Ile795=
NM_001324401.1:c.2329_2330delinsAT	NP_001311330.1:p.Ile777=
NM_001324402.1:c.1039_1040delinsAT	NP_001311331.1:p.Ile347=
XR_001744772.1:n.2495+835_2495+836delinsAT
NM_001127500.3:c.2383_2384delinsAT	NP_001120972.1:p.Ile795=
NM_000245.4:c.2329_2330delinsAT MANE Select	NP_000236.2:p.Ile777=
NM_001324401.2:c.2329_2330delinsAT	NP_001311330.1:p.Ile777=
NM_001324402.2:c.1039_1040delinsAT	NP_001311331.1:p.Ile347=
NM_001324401.3:c.2329_2330delinsAT	NP_001311330.1:p.Ile777=