Canonical Allele Identifier: CA1737025290

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759397G= , CM000669.2:g.116759397G=	GRCh38
NC_000007.13:g.116399451G= , CM000669.1:g.116399451G=	GRCh37
NC_000007.12:g.116186687G=	NCBI36
NG_008996.1:g.91993G= , LRG_662:g.91993G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2271G=	ENSP00000398776.2:p.Gly757=
ENST00000436117.3:c.2264+777G=	ENSP00000410980.2:n.2264+777G=
ENST00000318493.11:c.2325G=	ENSP00000317272.6:p.Gly775=
ENST00000397752.8:c.2271G= MANE Select	ENSP00000380860.3:p.Gly757=
ENST00000318493.10:c.2325G=	ENSP00000317272.6:p.Gly775=
ENST00000397752.7:c.2271G=	ENSP00000380860.3:p.Gly757=
ENST00000422097.1:c.111G=	ENSP00000398776.1:p.Gly37=
ENST00000436117.2:c.2264+777G=	ENSP00000410980.2:n.2264+777G=
NM_000245.2:c.2271G=	NP_000236.2:p.Gly757=
NM_001127500.1:c.2325G= , LRG_662t1:c.2325G=	NP_001120972.1:p.Gly775=
XM_006715990.2:c.981G=	XP_006716053.1:p.Gly327=
XM_006715991.2:c.981G=	XP_006716054.1:p.Gly327=
XM_011516223.1:c.2328G=	XP_011514525.1:p.Gly776=
NM_000245.3:c.2271G=	NP_000236.2:p.Gly757=
NM_001127500.2:c.2325G=	NP_001120972.1:p.Gly775=
NM_001324401.1:c.2271G=	NP_001311330.1:p.Gly757=
NM_001324402.1:c.981G=	NP_001311331.1:p.Gly327=
XR_001744772.1:n.2495+777G=
NM_001127500.3:c.2325G=	NP_001120972.1:p.Gly775=
NM_000245.4:c.2271G= MANE Select	NP_000236.2:p.Gly757=
NM_001324401.2:c.2271G=	NP_001311330.1:p.Gly757=
NM_001324402.2:c.981G=	NP_001311331.1:p.Gly327=
NM_001324401.3:c.2271G=	NP_001311330.1:p.Gly757=