Canonical Allele Identifier: CA368987499
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs867064468

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771983C>T , CM000669.2:g.116771983C>T GRCh38
NC_000007.13:g.116412037C>T , CM000669.1:g.116412037C>T GRCh37
NC_000007.12:g.116199273C>T NCBI36
NG_008996.1:g.104579C>T , LRG_662:g.104579C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*627C>T ENSP00000410980.2:n.*627C>T
ENST00000318493.11:c.3076C>T ENSP00000317272.6:p.Pro1026Ser
ENST00000397752.8:c.3022C>T MANE Select ENSP00000380860.3:p.Pro1008Ser
ENST00000318493.10:c.3076C>T ENSP00000317272.6:p.Pro1026Ser
ENST00000397752.7:c.3022C>T ENSP00000380860.3:p.Pro1008Ser
ENST00000454623.1:c.283+329C>T ENSP00000398140.1:n.283+329C>T
NM_000245.2:c.3022C>T NP_000236.2:p.Pro1008Ser
NM_001127500.1:c.3076C>T , LRG_662t1:c.3076C>T NP_001120972.1:p.Pro1026Ser
XM_006715990.2:c.1732C>T XP_006716053.1:p.Pro578Ser
XM_006715991.2:c.1732C>T XP_006716054.1:p.Pro578Ser
XM_011516223.1:c.3079C>T XP_011514525.1:p.Pro1027Ser
NM_000245.3:c.3022C>T NP_000236.2:p.Pro1008Ser
NM_001127500.2:c.3076C>T NP_001120972.1:p.Pro1026Ser
NM_001324402.1:c.1732C>T NP_001311331.1:p.Pro578Ser
XR_001744772.1:n.3153C>T
NM_001127500.3:c.3076C>T NP_001120972.1:p.Pro1026Ser
NM_000245.4:c.3022C>T MANE Select NP_000236.2:p.Pro1008Ser
NM_001324402.2:c.1732C>T NP_001311331.1:p.Pro578Ser