Canonical Allele Identifier: CA368986759

Gene: MET

Linked Data

• ClinVar Variation Id: 3232957
• ClinVar RCV Id: RCV004523589
• MyVariant Identifiers: chr7:g.116411694G>T (hg19) ; chr7:g.116771640G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771640G>T , CM000669.2:g.116771640G>T	GRCh38
NC_000007.13:g.116411694G>T , CM000669.1:g.116411694G>T	GRCh37
NC_000007.12:g.116198930G>T	NCBI36
NG_008996.1:g.104236G>T , LRG_662:g.104236G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*478G>T	ENSP00000410980.2:n.*478G>T
ENST00000318493.11:c.2927G>T	ENSP00000317272.6:p.Arg976Ile
ENST00000397752.8:c.2873G>T MANE Select	ENSP00000380860.3:p.Arg958Ile
ENST00000318493.10:c.2927G>T	ENSP00000317272.6:p.Arg976Ile
ENST00000397752.7:c.2873G>T	ENSP00000380860.3:p.Arg958Ile
ENST00000454623.1:c.269G>T	ENSP00000398140.1:p.Arg90Ile
NM_000245.2:c.2873G>T	NP_000236.2:p.Arg958Ile
NM_001127500.1:c.2927G>T , LRG_662t1:c.2927G>T	NP_001120972.1:p.Arg976Ile
XM_006715990.2:c.1583G>T	XP_006716053.1:p.Arg528Ile
XM_006715991.2:c.1583G>T	XP_006716054.1:p.Arg528Ile
XM_011516223.1:c.2930G>T	XP_011514525.1:p.Arg977Ile
NM_000245.3:c.2873G>T	NP_000236.2:p.Arg958Ile
NM_001127500.2:c.2927G>T	NP_001120972.1:p.Arg976Ile
NM_001324402.1:c.1583G>T	NP_001311331.1:p.Arg528Ile
XR_001744772.1:n.3004G>T
NM_001127500.3:c.2927G>T	NP_001120972.1:p.Arg976Ile
NM_000245.4:c.2873G>T MANE Select	NP_000236.2:p.Arg958Ile
NM_001324402.2:c.1583G>T	NP_001311331.1:p.Arg528Ile