Canonical Allele Identifier: CA368986748

Gene: MET

Linked Data

• ClinVar Variation Id: 1509000
• ClinVar RCV Id: RCV002016520
• dbSNP Id: rs1794836962
• MyVariant Identifiers: chr7:g.116411691A>T (hg19) ; chr7:g.116771637A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771637A>T , CM000669.2:g.116771637A>T	GRCh38
NC_000007.13:g.116411691A>T , CM000669.1:g.116411691A>T	GRCh37
NC_000007.12:g.116198927A>T	NCBI36
NG_008996.1:g.104233A>T , LRG_662:g.104233A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*475A>T	ENSP00000410980.2:n.*475A>T
ENST00000318493.11:c.2924A>T	ENSP00000317272.6:p.Lys975Met
ENST00000397752.8:c.2870A>T MANE Select	ENSP00000380860.3:p.Lys957Met
ENST00000318493.10:c.2924A>T	ENSP00000317272.6:p.Lys975Met
ENST00000397752.7:c.2870A>T	ENSP00000380860.3:p.Lys957Met
ENST00000454623.1:c.266A>T	ENSP00000398140.1:p.Lys89Met
NM_000245.2:c.2870A>T	NP_000236.2:p.Lys957Met
NM_001127500.1:c.2924A>T , LRG_662t1:c.2924A>T	NP_001120972.1:p.Lys975Met
XM_006715990.2:c.1580A>T	XP_006716053.1:p.Lys527Met
XM_006715991.2:c.1580A>T	XP_006716054.1:p.Lys527Met
XM_011516223.1:c.2927A>T	XP_011514525.1:p.Lys976Met
NM_000245.3:c.2870A>T	NP_000236.2:p.Lys957Met
NM_001127500.2:c.2924A>T	NP_001120972.1:p.Lys975Met
NM_001324402.1:c.1580A>T	NP_001311331.1:p.Lys527Met
XR_001744772.1:n.3001A>T
NM_001127500.3:c.2924A>T	NP_001120972.1:p.Lys975Met
NM_000245.4:c.2870A>T MANE Select	NP_000236.2:p.Lys957Met
NM_001324402.2:c.1580A>T	NP_001311331.1:p.Lys527Met