Canonical Allele Identifier: CA410693349
Gene: ARVCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19972369G>C , CM000684.2:g.19972369G>C GRCh38
NC_000022.10:g.19959892G>C , CM000684.1:g.19959892G>C GRCh37
NC_000022.9:g.18339892G>C NCBI36
NG_023326.1:g.49418C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263207.8:c.2684C>G MANE Select ENSP00000263207.3:p.Ala895Gly
ENST00000263207.7:c.2684C>G ENSP00000263207.3:p.Ala895Gly
ENST00000401994.5:c.2495C>G ENSP00000384341.1:p.Ala832Gly
ENST00000406259.1:c.2666C>G ENSP00000385444.1:p.Ala889Gly
ENST00000406522.5:c.2477C>G ENSP00000384732.1:p.Ala826Gly
ENST00000495096.5:n.1606C>G
NM_001670.2:c.2684C>G NP_001661.1:p.Ala895Gly
XM_005261242.1:c.2666C>G XP_005261299.1:p.Ala889Gly
XM_005261243.3:c.2666C>G XP_005261300.1:p.Ala889Gly
XM_005261244.3:c.2666C>G XP_005261301.1:p.Ala889Gly
XM_006724243.1:c.2684C>G XP_006724306.1:p.Ala895Gly
XM_006724245.2:c.2684C>G XP_006724308.1:p.Ala895Gly
XM_006724246.2:c.2438C>G XP_006724309.1:p.Ala813Gly
XM_006724247.2:c.2495C>G XP_006724310.1:p.Ala832Gly
XM_006724248.2:c.2477C>G XP_006724311.1:p.Ala826Gly
XM_011530179.1:c.2651C>G XP_011528481.1:p.Ala884Gly
XM_011530180.1:c.2684C>G XP_011528482.1:p.Ala895Gly
XM_011530182.1:c.1250C>G XP_011528484.1:p.Ala417Gly
XM_011530183.1:c.1232C>G XP_011528485.1:p.Ala411Gly
XR_937863.1:n.2771C>G
XR_937864.1:n.2771C>G
XM_005261242.3:c.2666C>G XP_005261299.1:p.Ala889Gly
XM_005261243.4:c.2666C>G XP_005261300.1:p.Ala889Gly
XM_005261244.4:c.2666C>G XP_005261301.1:p.Ala889Gly
XM_006724243.3:c.2684C>G XP_006724306.1:p.Ala895Gly
XM_006724245.3:c.2684C>G XP_006724308.1:p.Ala895Gly
XM_006724246.4:c.2438C>G XP_006724309.1:p.Ala813Gly
XM_006724247.4:c.2495C>G XP_006724310.1:p.Ala832Gly
XM_006724248.4:c.2477C>G XP_006724311.1:p.Ala826Gly
XM_011530179.3:c.2651C>G XP_011528481.1:p.Ala884Gly
XM_011530182.3:c.1250C>G XP_011528484.1:p.Ala417Gly
XM_011530183.3:c.1232C>G XP_011528485.1:p.Ala411Gly
XM_024452249.1:c.2438C>G XP_024308017.1:p.Ala813Gly
XR_937863.2:n.2771C>G
NM_001670.3:c.2684C>G MANE Select NP_001661.1:p.Ala895Gly