Canonical Allele Identifier: CA368987262

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116411986C>A (hg19) ; chr7:g.116771932C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771932C>A , CM000669.2:g.116771932C>A	GRCh38
NC_000007.13:g.116411986C>A , CM000669.1:g.116411986C>A	GRCh37
NC_000007.12:g.116199222C>A	NCBI36
NG_008996.1:g.104528C>A , LRG_662:g.104528C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*576C>A	ENSP00000410980.2:n.*576C>A
ENST00000318493.11:c.3025C>A	ENSP00000317272.6:p.Pro1009Thr
ENST00000397752.8:c.2971C>A MANE Select	ENSP00000380860.3:p.Pro991Thr
ENST00000318493.10:c.3025C>A	ENSP00000317272.6:p.Pro1009Thr
ENST00000397752.7:c.2971C>A	ENSP00000380860.3:p.Pro991Thr
ENST00000454623.1:c.283+278C>A	ENSP00000398140.1:n.283+278C>A
NM_000245.2:c.2971C>A	NP_000236.2:p.Pro991Thr
NM_001127500.1:c.3025C>A , LRG_662t1:c.3025C>A	NP_001120972.1:p.Pro1009Thr
XM_006715990.2:c.1681C>A	XP_006716053.1:p.Pro561Thr
XM_006715991.2:c.1681C>A	XP_006716054.1:p.Pro561Thr
XM_011516223.1:c.3028C>A	XP_011514525.1:p.Pro1010Thr
NM_000245.3:c.2971C>A	NP_000236.2:p.Pro991Thr
NM_001127500.2:c.3025C>A	NP_001120972.1:p.Pro1009Thr
NM_001324402.1:c.1681C>A	NP_001311331.1:p.Pro561Thr
XR_001744772.1:n.3102C>A
NM_001127500.3:c.3025C>A	NP_001120972.1:p.Pro1009Thr
NM_000245.4:c.2971C>A MANE Select	NP_000236.2:p.Pro991Thr
NM_001324402.2:c.1681C>A	NP_001311331.1:p.Pro561Thr