Canonical Allele Identifier: CA368968461

Gene: MET

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116699241C>A , CM000669.2:g.116699241C>A	GRCh38
NC_000007.13:g.116339295C>A , CM000669.1:g.116339295C>A	GRCh37
NC_000007.12:g.116126531C>A	NCBI36
NG_008996.1:g.31837C>A , LRG_662:g.31837C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.157C>A	ENSP00000398776.2:p.Gln53Lys
ENST00000436117.3:c.157C>A	ENSP00000410980.2:p.Gln53Lys
ENST00000318493.11:c.157C>A	ENSP00000317272.6:p.Gln53Lys
ENST00000397752.8:c.157C>A MANE Select	ENSP00000380860.3:p.Gln53Lys
ENST00000318493.10:c.157C>A	ENSP00000317272.6:p.Gln53Lys
ENST00000397752.7:c.157C>A	ENSP00000380860.3:p.Gln53Lys
ENST00000436117.2:c.157C>A	ENSP00000410980.2:p.Gln53Lys
ENST00000456159.1:c.214C>A	ENSP00000413857.1:p.Gln72Lys
NM_000245.2:c.157C>A	NP_000236.2:p.Gln53Lys
NM_001127500.1:c.157C>A , LRG_662t1:c.157C>A	NP_001120972.1:p.Gln53Lys
XM_006715991.2:c.-91+26664C>A	XP_006716054.1:n.-91+26664C>A
XM_011516223.1:c.214C>A	XP_011514525.1:p.Gln72Lys
NM_000245.3:c.157C>A	NP_000236.2:p.Gln53Lys
NM_001127500.2:c.157C>A	NP_001120972.1:p.Gln53Lys
NM_001324401.1:c.157C>A	NP_001311330.1:p.Gln53Lys
NM_001324402.1:c.-91+26664C>A	NP_001311331.1:n.-91+26664C>A
XR_001744772.1:n.388C>A
NM_001127500.3:c.157C>A	NP_001120972.1:p.Gln53Lys
NM_000245.4:c.157C>A MANE Select	NP_000236.2:p.Gln53Lys
NM_001324401.2:c.157C>A	NP_001311330.1:p.Gln53Lys
NM_001324402.2:c.-91+26664C>A	NP_001311331.1:n.-91+26664C>A
NM_001324401.3:c.157C>A	NP_001311330.1:p.Gln53Lys