Canonical Allele Identifier: CA368982003

Gene: MET

Linked Data

• ClinVar Variation Id: 1789782
• ClinVar RCV Id: RCV002448237
• dbSNP Id: rs2116937765
• MyVariant Identifiers: chr7:g.116399462C>T (hg19) ; chr7:g.116759408C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759408C>T , CM000669.2:g.116759408C>T	GRCh38
NC_000007.13:g.116399462C>T , CM000669.1:g.116399462C>T	GRCh37
NC_000007.12:g.116186698C>T	NCBI36
NG_008996.1:g.92004C>T , LRG_662:g.92004C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2282C>T	ENSP00000398776.2:p.Thr761Ile
ENST00000436117.3:c.2264+788C>T	ENSP00000410980.2:n.2264+788C>T
ENST00000318493.11:c.2336C>T	ENSP00000317272.6:p.Thr779Ile
ENST00000397752.8:c.2282C>T MANE Select	ENSP00000380860.3:p.Thr761Ile
ENST00000318493.10:c.2336C>T	ENSP00000317272.6:p.Thr779Ile
ENST00000397752.7:c.2282C>T	ENSP00000380860.3:p.Thr761Ile
ENST00000422097.1:c.122C>T	ENSP00000398776.1:p.Thr41Ile
ENST00000436117.2:c.2264+788C>T	ENSP00000410980.2:n.2264+788C>T
NM_000245.2:c.2282C>T	NP_000236.2:p.Thr761Ile
NM_001127500.1:c.2336C>T , LRG_662t1:c.2336C>T	NP_001120972.1:p.Thr779Ile
XM_006715990.2:c.992C>T	XP_006716053.1:p.Thr331Ile
XM_006715991.2:c.992C>T	XP_006716054.1:p.Thr331Ile
XM_011516223.1:c.2339C>T	XP_011514525.1:p.Thr780Ile
NM_000245.3:c.2282C>T	NP_000236.2:p.Thr761Ile
NM_001127500.2:c.2336C>T	NP_001120972.1:p.Thr779Ile
NM_001324401.1:c.2282C>T	NP_001311330.1:p.Thr761Ile
NM_001324402.1:c.992C>T	NP_001311331.1:p.Thr331Ile
XR_001744772.1:n.2495+788C>T
NM_001127500.3:c.2336C>T	NP_001120972.1:p.Thr779Ile
NM_000245.4:c.2282C>T MANE Select	NP_000236.2:p.Thr761Ile
NM_001324401.2:c.2282C>T	NP_001311330.1:p.Thr761Ile
NM_001324402.2:c.992C>T	NP_001311331.1:p.Thr331Ile
NM_001324401.3:c.2282C>T	NP_001311330.1:p.Thr761Ile