Canonical Allele Identifier: CA368989624

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116417472T>A (hg19) ; chr7:g.116777418T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116777418T>A , CM000669.2:g.116777418T>A	GRCh38
NC_000007.13:g.116417472T>A , CM000669.1:g.116417472T>A	GRCh37
NC_000007.12:g.116204708T>A	NCBI36
NG_008996.1:g.110014T>A , LRG_662:g.110014T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*894T>A	ENSP00000410980.2:n.*894T>A
ENST00000318493.11:c.3343T>A	ENSP00000317272.6:p.Leu1115Met
ENST00000397752.8:c.3289T>A MANE Select	ENSP00000380860.3:p.Leu1097Met
ENST00000318493.10:c.3343T>A	ENSP00000317272.6:p.Leu1115Met
ENST00000397752.7:c.3289T>A	ENSP00000380860.3:p.Leu1097Met
NM_000245.2:c.3289T>A	NP_000236.2:p.Leu1097Met
NM_001127500.1:c.3343T>A , LRG_662t1:c.3343T>A	NP_001120972.1:p.Leu1115Met
XM_006715990.2:c.1999T>A	XP_006716053.1:p.Leu667Met
XM_006715991.2:c.1999T>A	XP_006716054.1:p.Leu667Met
XM_011516223.1:c.3346T>A	XP_011514525.1:p.Leu1116Met
NM_000245.3:c.3289T>A	NP_000236.2:p.Leu1097Met
NM_001127500.2:c.3343T>A	NP_001120972.1:p.Leu1115Met
NM_001324402.1:c.1999T>A	NP_001311331.1:p.Leu667Met
XR_001744772.1:n.3420T>A
NM_001127500.3:c.3343T>A	NP_001120972.1:p.Leu1115Met
NM_000245.4:c.3289T>A MANE Select	NP_000236.2:p.Leu1097Met
NM_001324402.2:c.1999T>A	NP_001311331.1:p.Leu667Met