Canonical Allele Identifier: CA368987222

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116411977A>G (hg19) ; chr7:g.116771923A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771923A>G , CM000669.2:g.116771923A>G	GRCh38
NC_000007.13:g.116411977A>G , CM000669.1:g.116411977A>G	GRCh37
NC_000007.12:g.116199213A>G	NCBI36
NG_008996.1:g.104519A>G , LRG_662:g.104519A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*567A>G	ENSP00000410980.2:n.*567A>G
ENST00000318493.11:c.3016A>G	ENSP00000317272.6:p.Ser1006Gly
ENST00000397752.8:c.2962A>G MANE Select	ENSP00000380860.3:p.Ser988Gly
ENST00000318493.10:c.3016A>G	ENSP00000317272.6:p.Ser1006Gly
ENST00000397752.7:c.2962A>G	ENSP00000380860.3:p.Ser988Gly
ENST00000454623.1:c.283+269A>G	ENSP00000398140.1:n.283+269A>G
NM_000245.2:c.2962A>G	NP_000236.2:p.Ser988Gly
NM_001127500.1:c.3016A>G , LRG_662t1:c.3016A>G	NP_001120972.1:p.Ser1006Gly
XM_006715990.2:c.1672A>G	XP_006716053.1:p.Ser558Gly
XM_006715991.2:c.1672A>G	XP_006716054.1:p.Ser558Gly
XM_011516223.1:c.3019A>G	XP_011514525.1:p.Ser1007Gly
NM_000245.3:c.2962A>G	NP_000236.2:p.Ser988Gly
NM_001127500.2:c.3016A>G	NP_001120972.1:p.Ser1006Gly
NM_001324402.1:c.1672A>G	NP_001311331.1:p.Ser558Gly
XR_001744772.1:n.3093A>G
NM_001127500.3:c.3016A>G	NP_001120972.1:p.Ser1006Gly
NM_000245.4:c.2962A>G MANE Select	NP_000236.2:p.Ser988Gly
NM_001324402.2:c.1672A>G	NP_001311331.1:p.Ser558Gly