Canonical Allele Identifier: CA10105104
Gene: ARVCF HGNC NCBI

Linked Data

dbSNP Id: rs114991369

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19973013G>A , CM000684.2:g.19973013G>A GRCh38
NC_000022.10:g.19960536G>A , CM000684.1:g.19960536G>A GRCh37
NC_000022.9:g.18340536G>A NCBI36
NG_023326.1:g.48774C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263207.8:c.2462C>T MANE Select ENSP00000263207.3:p.Ala821Val
ENST00000263207.7:c.2462C>T ENSP00000263207.3:p.Ala821Val
ENST00000401994.5:c.2273C>T ENSP00000384341.1:p.Ala758Val
ENST00000406259.1:c.2444C>T ENSP00000385444.1:p.Ala815Val
ENST00000406522.5:c.2255C>T ENSP00000384732.1:p.Ala752Val
ENST00000495096.5:n.1384C>T
NM_001670.2:c.2462C>T NP_001661.1:p.Ala821Val
XM_005261242.1:c.2444C>T XP_005261299.1:p.Ala815Val
XM_005261243.3:c.2444C>T XP_005261300.1:p.Ala815Val
XM_005261244.3:c.2444C>T XP_005261301.1:p.Ala815Val
XM_006724243.1:c.2462C>T XP_006724306.1:p.Ala821Val
XM_006724245.2:c.2462C>T XP_006724308.1:p.Ala821Val
XM_006724246.2:c.2216C>T XP_006724309.1:p.Ala739Val
XM_006724247.2:c.2273C>T XP_006724310.1:p.Ala758Val
XM_006724248.2:c.2255C>T XP_006724311.1:p.Ala752Val
XM_011530179.1:c.2429C>T XP_011528481.1:p.Ala810Val
XM_011530180.1:c.2462C>T XP_011528482.1:p.Ala821Val
XM_011530182.1:c.1028C>T XP_011528484.1:p.Ala343Val
XM_011530183.1:c.1010C>T XP_011528485.1:p.Ala337Val
XR_937863.1:n.2549C>T
XR_937864.1:n.2549C>T
XM_005261242.3:c.2444C>T XP_005261299.1:p.Ala815Val
XM_005261243.4:c.2444C>T XP_005261300.1:p.Ala815Val
XM_005261244.4:c.2444C>T XP_005261301.1:p.Ala815Val
XM_006724243.3:c.2462C>T XP_006724306.1:p.Ala821Val
XM_006724245.3:c.2462C>T XP_006724308.1:p.Ala821Val
XM_006724246.4:c.2216C>T XP_006724309.1:p.Ala739Val
XM_006724247.4:c.2273C>T XP_006724310.1:p.Ala758Val
XM_006724248.4:c.2255C>T XP_006724311.1:p.Ala752Val
XM_011530179.3:c.2429C>T XP_011528481.1:p.Ala810Val
XM_011530182.3:c.1028C>T XP_011528484.1:p.Ala343Val
XM_011530183.3:c.1010C>T XP_011528485.1:p.Ala337Val
XM_024452249.1:c.2216C>T XP_024308017.1:p.Ala739Val
XR_937863.2:n.2549C>T
NM_001670.3:c.2462C>T MANE Select NP_001661.1:p.Ala821Val