Canonical Allele Identifier: CA457216240

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116395481A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116755427A>C , CM000669.2:g.116755427A>C	GRCh38
NC_000007.13:g.116395481A>C , CM000669.1:g.116395481A>C	GRCh37
NC_000007.12:g.116182717A>C	NCBI36
NG_008996.1:g.88023A>C , LRG_662:g.88023A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.1774A>C	ENSP00000398776.2:p.Arg592=
ENST00000436117.3:c.1774A>C	ENSP00000410980.2:p.Arg592=
ENST00000318493.11:c.1774A>C	ENSP00000317272.6:p.Arg592=
ENST00000397752.8:c.1774A>C MANE Select	ENSP00000380860.3:p.Arg592=
ENST00000318493.10:c.1774A>C	ENSP00000317272.6:p.Arg592=
ENST00000397752.7:c.1774A>C	ENSP00000380860.3:p.Arg592=
ENST00000436117.2:c.1774A>C	ENSP00000410980.2:p.Arg592=
NM_000245.2:c.1774A>C	NP_000236.2:p.Arg592=
NM_001127500.1:c.1774A>C , LRG_662t1:c.1774A>C	NP_001120972.1:p.Arg592=
XM_006715990.2:c.484A>C	XP_006716053.1:p.Arg162=
XM_006715991.2:c.484A>C	XP_006716054.1:p.Arg162=
XM_011516223.1:c.1831A>C	XP_011514525.1:p.Arg611=
NM_000245.3:c.1774A>C	NP_000236.2:p.Arg592=
NM_001127500.2:c.1774A>C	NP_001120972.1:p.Arg592=
NM_001324401.1:c.1774A>C	NP_001311330.1:p.Arg592=
NM_001324402.1:c.484A>C	NP_001311331.1:p.Arg162=
XR_001744772.1:n.2005A>C
NM_001127500.3:c.1774A>C	NP_001120972.1:p.Arg592=
NM_000245.4:c.1774A>C MANE Select	NP_000236.2:p.Arg592=
NM_001324401.2:c.1774A>C	NP_001311330.1:p.Arg592=
NM_001324402.2:c.484A>C	NP_001311331.1:p.Arg162=
NM_001324401.3:c.1774A>C	NP_001311330.1:p.Arg592=