Canonical Allele Identifier: CA368983110

Gene: MET

Linked Data

• MyVariant Identifiers: chr7:g.116403162A>C (hg19) ; chr7:g.116763108A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116763108A>C , CM000669.2:g.116763108A>C	GRCh38
NC_000007.13:g.116403162A>C , CM000669.1:g.116403162A>C	GRCh37
NC_000007.12:g.116190398A>C	NCBI36
NG_008996.1:g.95704A>C , LRG_662:g.95704A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000422097.2:c.2423A>C	ENSP00000398776.2:p.Gln808Pro
ENST00000436117.3:c.*28A>C	ENSP00000410980.2:n.*28A>C
ENST00000318493.11:c.2477A>C	ENSP00000317272.6:p.Gln826Pro
ENST00000397752.8:c.2423A>C MANE Select	ENSP00000380860.3:p.Gln808Pro
ENST00000318493.10:c.2477A>C	ENSP00000317272.6:p.Gln826Pro
ENST00000397752.7:c.2423A>C	ENSP00000380860.3:p.Gln808Pro
ENST00000422097.1:c.263A>C	ENSP00000398776.1:p.Gln88Pro
NM_000245.2:c.2423A>C	NP_000236.2:p.Gln808Pro
NM_001127500.1:c.2477A>C , LRG_662t1:c.2477A>C	NP_001120972.1:p.Gln826Pro
XM_006715990.2:c.1133A>C	XP_006716053.1:p.Gln378Pro
XM_006715991.2:c.1133A>C	XP_006716054.1:p.Gln378Pro
XM_011516223.1:c.2480A>C	XP_011514525.1:p.Gln827Pro
NM_000245.3:c.2423A>C	NP_000236.2:p.Gln808Pro
NM_001127500.2:c.2477A>C	NP_001120972.1:p.Gln826Pro
NM_001324401.1:c.2423A>C	NP_001311330.1:p.Gln808Pro
NM_001324402.1:c.1133A>C	NP_001311331.1:p.Gln378Pro
XR_001744772.1:n.2554A>C
NM_001127500.3:c.2477A>C	NP_001120972.1:p.Gln826Pro
NM_000245.4:c.2423A>C MANE Select	NP_000236.2:p.Gln808Pro
NM_001324401.2:c.2423A>C	NP_001311330.1:p.Gln808Pro
NM_001324402.2:c.1133A>C	NP_001311331.1:p.Gln378Pro
NM_001324401.3:c.2423A>C	NP_001311330.1:p.Gln808Pro