Canonical Allele Identifier: CA1737012009

Gene: MET

Linked Data

• dbSNP Id: rs1795167291

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.116781937T>C , CM000669.2:g.116781937T>C	GRCh38
NC_000007.13:g.116421991T>C , CM000669.1:g.116421991T>C	GRCh37
NC_000007.12:g.116209227T>C	NCBI36
NG_008996.1:g.114533T>C , LRG_662:g.114533T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000436117.3:c.*1128-51T>C	ENSP00000410980.2:n.*1128-51T>C
ENST00000318493.11:c.3577-51T>C	ENSP00000317272.6:n.3577-51T>C
ENST00000397752.8:c.3523-51T>C MANE Select	ENSP00000380860.3:n.3523-51T>C
ENST00000318493.10:c.3577-51T>C	ENSP00000317272.6:n.3577-51T>C
ENST00000397752.7:c.3523-51T>C	ENSP00000380860.3:n.3523-51T>C
NM_000245.2:c.3523-51T>C	NP_000236.2:n.3523-51T>C
NM_001127500.1:c.3577-51T>C , LRG_662t1:c.3577-51T>C	NP_001120972.1:n.3577-51T>C
XM_006715990.2:c.2233-51T>C	XP_006716053.1:n.2233-51T>C
XM_006715991.2:c.2233-51T>C	XP_006716054.1:n.2233-51T>C
XM_011516223.1:c.3580-51T>C	XP_011514525.1:n.3580-51T>C
NM_000245.3:c.3523-51T>C	NP_000236.2:n.3523-51T>C
NM_001127500.2:c.3577-51T>C	NP_001120972.1:n.3577-51T>C
NM_001324402.1:c.2233-51T>C	NP_001311331.1:n.2233-51T>C
XR_001744772.1:n.3654-51T>C
NM_001127500.3:c.3577-51T>C	NP_001120972.1:n.3577-51T>C
NM_000245.4:c.3523-51T>C MANE Select	NP_000236.2:n.3523-51T>C
NM_001324402.2:c.2233-51T>C	NP_001311331.1:n.2233-51T>C