Canonical Allele Identifier: CA368989641

Gene: MET

Linked Data

• ClinVar Variation Id: 2428812
• ClinVar RCV Id: RCV003120413
• gnomAD v4: 7-116777422-T-C
• MyVariant Identifiers: chr7:g.116417476T>C (hg19) ; chr7:g.116777422T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116777422T>C , CM000669.2:g.116777422T>C	GRCh38
NC_000007.13:g.116417476T>C , CM000669.1:g.116417476T>C	GRCh37
NC_000007.12:g.116204712T>C	NCBI36
NG_008996.1:g.110018T>C , LRG_662:g.110018T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*898T>C	ENSP00000410980.2:n.*898T>C
ENST00000318493.11:c.3347T>C	ENSP00000317272.6:p.Leu1116Ser
ENST00000397752.8:c.3293T>C MANE Select	ENSP00000380860.3:p.Leu1098Ser
ENST00000318493.10:c.3347T>C	ENSP00000317272.6:p.Leu1116Ser
ENST00000397752.7:c.3293T>C	ENSP00000380860.3:p.Leu1098Ser
NM_000245.2:c.3293T>C	NP_000236.2:p.Leu1098Ser
NM_001127500.1:c.3347T>C , LRG_662t1:c.3347T>C	NP_001120972.1:p.Leu1116Ser
XM_006715990.2:c.2003T>C	XP_006716053.1:p.Leu668Ser
XM_006715991.2:c.2003T>C	XP_006716054.1:p.Leu668Ser
XM_011516223.1:c.3350T>C	XP_011514525.1:p.Leu1117Ser
NM_000245.3:c.3293T>C	NP_000236.2:p.Leu1098Ser
NM_001127500.2:c.3347T>C	NP_001120972.1:p.Leu1116Ser
NM_001324402.1:c.2003T>C	NP_001311331.1:p.Leu668Ser
XR_001744772.1:n.3424T>C
NM_001127500.3:c.3347T>C	NP_001120972.1:p.Leu1116Ser
NM_000245.4:c.3293T>C MANE Select	NP_000236.2:p.Leu1098Ser
NM_001324402.2:c.2003T>C	NP_001311331.1:p.Leu668Ser