Canonical Allele Identifier: CA1737000201

Gene: MET

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116697595G= , CM000669.2:g.116697595G=	GRCh38
NC_000007.13:g.116337649G= , CM000669.1:g.116337649G=	GRCh37
NC_000007.12:g.116124885G=	NCBI36
NG_008996.1:g.30191G= , LRG_662:g.30191G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.-14-1476G=	ENSP00000398776.2:n.-14-1476G=
ENST00000436117.3:c.-14-1476G=	ENSP00000410980.2:n.-14-1476G=
ENST00000318493.11:c.-14-1476G=	ENSP00000317272.6:n.-14-1476G=
ENST00000397752.8:c.-14-1476G= MANE Select	ENSP00000380860.3:n.-14-1476G=
ENST00000318493.10:c.-14-1476G=	ENSP00000317272.6:n.-14-1476G=
ENST00000397752.7:c.-14-1476G=	ENSP00000380860.3:n.-14-1476G=
ENST00000456159.1:c.44-1476G=	ENSP00000413857.1:n.44-1476G=
NM_000245.2:c.-14-1476G=	NP_000236.2:n.-14-1476G=
NM_001127500.1:c.-14-1476G= , LRG_662t1:c.-14-1476G=	NP_001120972.1:n.-14-1476G=
XM_006715991.2:c.-91+25018G=	XP_006716054.1:n.-91+25018G=
XM_011516223.1:c.44-1476G=	XP_011514525.1:n.44-1476G=
NM_000245.3:c.-14-1476G=	NP_000236.2:n.-14-1476G=
NM_001127500.2:c.-14-1476G=	NP_001120972.1:n.-14-1476G=
NM_001324401.1:c.-14-1476G=	NP_001311330.1:n.-14-1476G=
NM_001324402.1:c.-91+25018G=	NP_001311331.1:n.-91+25018G=
XR_001744772.1:n.218-1476G=
NM_001127500.3:c.-14-1476G=	NP_001120972.1:n.-14-1476G=
NM_000245.4:c.-14-1476G= MANE Select	NP_000236.2:n.-14-1476G=
NM_001324401.2:c.-14-1476G=	NP_001311330.1:n.-14-1476G=
NM_001324402.2:c.-91+25018G=	NP_001311331.1:n.-91+25018G=
NM_001324401.3:c.-14-1476G=	NP_001311330.1:n.-14-1476G=