Canonical Allele Identifier: CA399558893
Gene: RAB5C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42128777A>C , CM000679.2:g.42128777A>C GRCh38
NC_000017.10:g.40280795A>C , CM000679.1:g.40280795A>C GRCh37
NC_000017.9:g.37534321A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000346213.9:c.190T>G MANE Select ENSP00000345689.5:p.Cys64Gly
ENST00000346213.8:c.190T>G ENSP00000345689.4:p.Cys64Gly
ENST00000393860.7:c.190T>G ENSP00000377440.3:p.Cys64Gly
ENST00000546881.1:n.382T>G
ENST00000547517.5:c.289T>G ENSP00000447053.1:p.Cys97Gly
ENST00000550406.1:c.190T>G ENSP00000448314.1:p.Cys64Gly
ENST00000550504.5:c.190T>G ENSP00000449777.1:p.Cys64Gly
ENST00000552162.5:c.190T>G ENSP00000449612.1:p.Cys64Gly
ENST00000592248.5:c.190T>G ENSP00000468275.1:p.Cys64Gly
ENST00000592574.1:c.190T>G ENSP00000468367.1:p.Cys64Gly
NM_001252039.1:c.289T>G NP_001238968.1:p.Cys97Gly
NM_004583.3:c.190T>G NP_004574.2:p.Cys64Gly
NM_201434.2:c.190T>G NP_958842.1:p.Cys64Gly
XM_011525090.1:c.190T>G XP_011523392.1:p.Cys64Gly
XM_011525091.1:c.190T>G XP_011523393.1:p.Cys64Gly
NM_001252039.2:c.289T>G NP_001238968.1:p.Cys97Gly
NM_004583.4:c.190T>G MANE Select NP_004574.2:p.Cys64Gly
NM_201434.3:c.190T>G NP_958842.1:p.Cys64Gly