Canonical Allele Identifier: CA2715553396
Gene: MET HGNC NCBI

Linked Data

dbSNP Id: rs2116997857

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.116771983_116771994delinsG , CM000669.2:g.116771983_116771994delinsG GRCh38
NC_000007.13:g.116412037_116412048delinsG , CM000669.1:g.116412037_116412048delinsG GRCh37
NC_000007.12:g.116199273_116199284delinsG NCBI36
NG_008996.1:g.104579_104590delinsG , LRG_662:g.104579_104590delinsG

Transcript Alleles

HGVS Amino-acid Change
ENST00000436117.3:c.*627_*633+5delinsG
ENST00000318493.11:c.3076_3082+5delinsG
ENST00000397752.8:c.3022_3028+5delinsG
ENST00000318493.10:c.3076_3082+5delinsG
ENST00000397752.7:c.3022_3028+5delinsG
ENST00000454623.1:c.283+329_283+340delinsG ENSP00000398140.1:n.283+329_283+340delinsG
NM_000245.2:c.3022_3028+5delinsG
NM_001127500.1:c.3076_3082+5delinsG , LRG_662t1:c.3076_3082+5delinsG
XM_006715990.2:c.1732_1738+5delinsG
XM_006715991.2:c.1732_1738+5delinsG
XM_011516223.1:c.3079_3085+5delinsG
NM_000245.3:c.3022_3028+5delinsG
NM_001127500.2:c.3076_3082+5delinsG
NM_001324402.1:c.1732_1738+5delinsG
XR_001744772.1:n.3153_3159+5delinsG
NM_001127500.3:c.3076_3082+5delinsG
NM_000245.4:c.3022_3028+5delinsG
NM_001324402.2:c.1732_1738+5delinsG