Canonical Allele Identifier: CA368991380

Gene: MET

Linked Data

• dbSNP Id: rs1795206855
• MyVariant Identifiers: chr7:g.116423363A>T (hg19) ; chr7:g.116783309A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783309A>T , CM000669.2:g.116783309A>T	GRCh38
NC_000007.13:g.116423363A>T , CM000669.1:g.116423363A>T	GRCh37
NC_000007.12:g.116210599A>T	NCBI36
NG_008996.1:g.115905A>T , LRG_662:g.115905A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*1243A>T	ENSP00000410980.2:n.*1243A>T
ENST00000318493.11:c.3692A>T	ENSP00000317272.6:p.Asp1231Val
ENST00000397752.8:c.3638A>T MANE Select	ENSP00000380860.3:p.Asp1213Val
ENST00000318493.10:c.3692A>T	ENSP00000317272.6:p.Asp1231Val
ENST00000397752.7:c.3638A>T	ENSP00000380860.3:p.Asp1213Val
NM_000245.2:c.3638A>T	NP_000236.2:p.Asp1213Val
NM_001127500.1:c.3692A>T , LRG_662t1:c.3692A>T	NP_001120972.1:p.Asp1231Val
XM_006715990.2:c.2348A>T	XP_006716053.1:p.Asp783Val
XM_006715991.2:c.2348A>T	XP_006716054.1:p.Asp783Val
XM_011516223.1:c.3695A>T	XP_011514525.1:p.Asp1232Val
NM_000245.3:c.3638A>T	NP_000236.2:p.Asp1213Val
NM_001127500.2:c.3692A>T	NP_001120972.1:p.Asp1231Val
NM_001324402.1:c.2348A>T	NP_001311331.1:p.Asp783Val
XR_001744772.1:n.3769A>T
NM_001127500.3:c.3692A>T	NP_001120972.1:p.Asp1231Val
NM_000245.4:c.3638A>T MANE Select	NP_000236.2:p.Asp1213Val
NM_001324402.2:c.2348A>T	NP_001311331.1:p.Asp783Val