Canonical Allele Identifier: CA1737025042

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759294C= , CM000669.2:g.116759294C=	GRCh38
NC_000007.13:g.116399348C= , CM000669.1:g.116399348C=	GRCh37
NC_000007.12:g.116186584C=	NCBI36
NG_008996.1:g.91890C= , LRG_662:g.91890C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2265-97C=	ENSP00000398776.2:n.2265-97C=
ENST00000436117.3:c.2264+674C=	ENSP00000410980.2:n.2264+674C=
ENST00000318493.11:c.2265-43C=	ENSP00000317272.6:n.2265-43C=
ENST00000397752.8:c.2265-97C= MANE Select	ENSP00000380860.3:n.2265-97C=
ENST00000318493.10:c.2265-43C=	ENSP00000317272.6:n.2265-43C=
ENST00000397752.7:c.2265-97C=	ENSP00000380860.3:n.2265-97C=
ENST00000422097.1:c.105-97C=	ENSP00000398776.1:n.105-97C=
ENST00000436117.2:c.2264+674C=	ENSP00000410980.2:n.2264+674C=
NM_000245.2:c.2265-97C=	NP_000236.2:n.2265-97C=
NM_001127500.1:c.2265-43C= , LRG_662t1:c.2265-43C=	NP_001120972.1:n.2265-43C=
XM_006715990.2:c.975-97C=	XP_006716053.1:n.975-97C=
XM_006715991.2:c.975-97C=	XP_006716054.1:n.975-97C=
XM_011516223.1:c.2322-97C=	XP_011514525.1:n.2322-97C=
NM_000245.3:c.2265-97C=	NP_000236.2:n.2265-97C=
NM_001127500.2:c.2265-43C=	NP_001120972.1:n.2265-43C=
NM_001324401.1:c.2265-97C=	NP_001311330.1:n.2265-97C=
NM_001324402.1:c.975-97C=	NP_001311331.1:n.975-97C=
XR_001744772.1:n.2495+674C=
NM_001127500.3:c.2265-43C=	NP_001120972.1:n.2265-43C=
NM_000245.4:c.2265-97C= MANE Select	NP_000236.2:n.2265-97C=
NM_001324401.2:c.2265-97C=	NP_001311330.1:n.2265-97C=
NM_001324402.2:c.975-97C=	NP_001311331.1:n.975-97C=
NM_001324401.3:c.2265-97C=	NP_001311330.1:n.2265-97C=