Canonical Allele Identifier: CA368987112

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116411952T>G (hg19) ; chr7:g.116771898T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771898T>G , CM000669.2:g.116771898T>G	GRCh38
NC_000007.13:g.116411952T>G , CM000669.1:g.116411952T>G	GRCh37
NC_000007.12:g.116199188T>G	NCBI36
NG_008996.1:g.104494T>G , LRG_662:g.104494T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*542T>G	ENSP00000410980.2:n.*542T>G
ENST00000318493.11:c.2991T>G	ENSP00000317272.6:p.His997Gln
ENST00000397752.8:c.2937T>G MANE Select	ENSP00000380860.3:p.His979Gln
ENST00000318493.10:c.2991T>G	ENSP00000317272.6:p.His997Gln
ENST00000397752.7:c.2937T>G	ENSP00000380860.3:p.His979Gln
ENST00000454623.1:c.283+244T>G	ENSP00000398140.1:n.283+244T>G
NM_000245.2:c.2937T>G	NP_000236.2:p.His979Gln
NM_001127500.1:c.2991T>G , LRG_662t1:c.2991T>G	NP_001120972.1:p.His997Gln
XM_006715990.2:c.1647T>G	XP_006716053.1:p.His549Gln
XM_006715991.2:c.1647T>G	XP_006716054.1:p.His549Gln
XM_011516223.1:c.2994T>G	XP_011514525.1:p.His998Gln
NM_000245.3:c.2937T>G	NP_000236.2:p.His979Gln
NM_001127500.2:c.2991T>G	NP_001120972.1:p.His997Gln
NM_001324402.1:c.1647T>G	NP_001311331.1:p.His549Gln
XR_001744772.1:n.3068T>G
NM_001127500.3:c.2991T>G	NP_001120972.1:p.His997Gln
NM_000245.4:c.2937T>G MANE Select	NP_000236.2:p.His979Gln
NM_001324402.2:c.1647T>G	NP_001311331.1:p.His549Gln