Canonical Allele Identifier: CA4448607

Gene: MET

Linked Data

• dbSNP Id: rs767720971
• ExAC: 7:116411870 T / C
• gnomAD v2: 7-116411870-T-C
• MyVariant Identifiers: chr7:g.116411870T>C (hg19) ; chr7:g.116771816T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116771816T>C , CM000669.2:g.116771816T>C	GRCh38
NC_000007.13:g.116411870T>C , CM000669.1:g.116411870T>C	GRCh37
NC_000007.12:g.116199106T>C	NCBI36
NG_008996.1:g.104412T>C , LRG_662:g.104412T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000436117.3:c.*493-33T>C	ENSP00000410980.2:n.*493-33T>C
ENST00000318493.11:c.2942-33T>C	ENSP00000317272.6:n.2942-33T>C
ENST00000397752.8:c.2888-33T>C MANE Select	ENSP00000380860.3:n.2888-33T>C
ENST00000318493.10:c.2942-33T>C	ENSP00000317272.6:n.2942-33T>C
ENST00000397752.7:c.2888-33T>C	ENSP00000380860.3:n.2888-33T>C
ENST00000454623.1:c.283+162T>C	ENSP00000398140.1:n.283+162T>C
NM_000245.2:c.2888-33T>C	NP_000236.2:n.2888-33T>C
NM_001127500.1:c.2942-33T>C , LRG_662t1:c.2942-33T>C	NP_001120972.1:n.2942-33T>C
XM_006715990.2:c.1598-33T>C	XP_006716053.1:n.1598-33T>C
XM_006715991.2:c.1598-33T>C	XP_006716054.1:n.1598-33T>C
XM_011516223.1:c.2945-33T>C	XP_011514525.1:n.2945-33T>C
NM_000245.3:c.2888-33T>C	NP_000236.2:n.2888-33T>C
NM_001127500.2:c.2942-33T>C	NP_001120972.1:n.2942-33T>C
NM_001324402.1:c.1598-33T>C	NP_001311331.1:n.1598-33T>C
XR_001744772.1:n.3019-33T>C
NM_001127500.3:c.2942-33T>C	NP_001120972.1:n.2942-33T>C
NM_000245.4:c.2888-33T>C MANE Select	NP_000236.2:n.2888-33T>C
NM_001324402.2:c.1598-33T>C	NP_001311331.1:n.1598-33T>C