Canonical Allele Identifier: CA368982315

Gene: MET

Linked Data

• dbSNP Id: rs2116938395
• MyVariant Identifiers: chr7:g.116399497C>G (hg19) ; chr7:g.116759443C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116759443C>G , CM000669.2:g.116759443C>G	GRCh38
NC_000007.13:g.116399497C>G , CM000669.1:g.116399497C>G	GRCh37
NC_000007.12:g.116186733C>G	NCBI36
NG_008996.1:g.92039C>G , LRG_662:g.92039C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000422097.2:c.2317C>G	ENSP00000398776.2:p.Pro773Ala
ENST00000436117.3:c.2264+823C>G	ENSP00000410980.2:n.2264+823C>G
ENST00000318493.11:c.2371C>G	ENSP00000317272.6:p.Pro791Ala
ENST00000397752.8:c.2317C>G MANE Select	ENSP00000380860.3:p.Pro773Ala
ENST00000318493.10:c.2371C>G	ENSP00000317272.6:p.Pro791Ala
ENST00000397752.7:c.2317C>G	ENSP00000380860.3:p.Pro773Ala
ENST00000422097.1:c.157C>G	ENSP00000398776.1:p.Pro53Ala
ENST00000436117.2:c.2264+823C>G	ENSP00000410980.2:n.2264+823C>G
NM_000245.2:c.2317C>G	NP_000236.2:p.Pro773Ala
NM_001127500.1:c.2371C>G , LRG_662t1:c.2371C>G	NP_001120972.1:p.Pro791Ala
XM_006715990.2:c.1027C>G	XP_006716053.1:p.Pro343Ala
XM_006715991.2:c.1027C>G	XP_006716054.1:p.Pro343Ala
XM_011516223.1:c.2374C>G	XP_011514525.1:p.Pro792Ala
NM_000245.3:c.2317C>G	NP_000236.2:p.Pro773Ala
NM_001127500.2:c.2371C>G	NP_001120972.1:p.Pro791Ala
NM_001324401.1:c.2317C>G	NP_001311330.1:p.Pro773Ala
NM_001324402.1:c.1027C>G	NP_001311331.1:p.Pro343Ala
XR_001744772.1:n.2495+823C>G
NM_001127500.3:c.2371C>G	NP_001120972.1:p.Pro791Ala
NM_000245.4:c.2317C>G MANE Select	NP_000236.2:p.Pro773Ala
NM_001324401.2:c.2317C>G	NP_001311330.1:p.Pro773Ala
NM_001324402.2:c.1027C>G	NP_001311331.1:p.Pro343Ala
NM_001324401.3:c.2317C>G	NP_001311330.1:p.Pro773Ala