Canonical Allele Identifier: CA368991593

Gene: MET

Linked Data

• dbSNP Id: rs121913247
• MyVariant Identifiers: chr7:g.116423413T>A (hg19) ; chr7:g.116783359T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116783359T>A , CM000669.2:g.116783359T>A	GRCh38
NC_000007.13:g.116423413T>A , CM000669.1:g.116423413T>A	GRCh37
NC_000007.12:g.116210649T>A	NCBI36
NG_008996.1:g.115955T>A , LRG_662:g.115955T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1293T>A	ENSP00000410980.2:n.*1293T>A
ENST00000318493.11:c.3742T>A	ENSP00000317272.6:p.Tyr1248Asn
ENST00000397752.8:c.3688T>A MANE Select	ENSP00000380860.3:p.Tyr1230Asn
ENST00000318493.10:c.3742T>A	ENSP00000317272.6:p.Tyr1248Asn
ENST00000397752.7:c.3688T>A	ENSP00000380860.3:p.Tyr1230Asn
NM_000245.2:c.3688T>A	NP_000236.2:p.Tyr1230Asn
NM_001127500.1:c.3742T>A , LRG_662t1:c.3742T>A	NP_001120972.1:p.Tyr1248Asn
XM_006715990.2:c.2398T>A	XP_006716053.1:p.Tyr800Asn
XM_006715991.2:c.2398T>A	XP_006716054.1:p.Tyr800Asn
XM_011516223.1:c.3745T>A	XP_011514525.1:p.Tyr1249Asn
NM_000245.3:c.3688T>A	NP_000236.2:p.Tyr1230Asn
NM_001127500.2:c.3742T>A	NP_001120972.1:p.Tyr1248Asn
NM_001324402.1:c.2398T>A	NP_001311331.1:p.Tyr800Asn
XR_001744772.1:n.3819T>A
NM_001127500.3:c.3742T>A	NP_001120972.1:p.Tyr1248Asn
NM_000245.4:c.3688T>A MANE Select	NP_000236.2:p.Tyr1230Asn
NM_001324402.2:c.2398T>A	NP_001311331.1:p.Tyr800Asn