Canonical Allele Identifier: CA368987078

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116411945C>A (hg19) ; chr7:g.116771891C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771891C>A , CM000669.2:g.116771891C>A	GRCh38
NC_000007.13:g.116411945C>A , CM000669.1:g.116411945C>A	GRCh37
NC_000007.12:g.116199181C>A	NCBI36
NG_008996.1:g.104487C>A , LRG_662:g.104487C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*535C>A	ENSP00000410980.2:n.*535C>A
ENST00000318493.11:c.2984C>A	ENSP00000317272.6:p.Thr995Asn
ENST00000397752.8:c.2930C>A MANE Select	ENSP00000380860.3:p.Thr977Asn
ENST00000318493.10:c.2984C>A	ENSP00000317272.6:p.Thr995Asn
ENST00000397752.7:c.2930C>A	ENSP00000380860.3:p.Thr977Asn
ENST00000454623.1:c.283+237C>A	ENSP00000398140.1:n.283+237C>A
NM_000245.2:c.2930C>A	NP_000236.2:p.Thr977Asn
NM_001127500.1:c.2984C>A , LRG_662t1:c.2984C>A	NP_001120972.1:p.Thr995Asn
XM_006715990.2:c.1640C>A	XP_006716053.1:p.Thr547Asn
XM_006715991.2:c.1640C>A	XP_006716054.1:p.Thr547Asn
XM_011516223.1:c.2987C>A	XP_011514525.1:p.Thr996Asn
NM_000245.3:c.2930C>A	NP_000236.2:p.Thr977Asn
NM_001127500.2:c.2984C>A	NP_001120972.1:p.Thr995Asn
NM_001324402.1:c.1640C>A	NP_001311331.1:p.Thr547Asn
XR_001744772.1:n.3061C>A
NM_001127500.3:c.2984C>A	NP_001120972.1:p.Thr995Asn
NM_000245.4:c.2930C>A MANE Select	NP_000236.2:p.Thr977Asn
NM_001324402.2:c.1640C>A	NP_001311331.1:p.Thr547Asn