Canonical Allele Identifier: CA2396130457
Gene: ARVCF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19972221_19972232delinsCTCACCCTCTAA , CM000684.2:g.19972221_19972232delinsCTCACCCTCTAA GRCh38
NC_000022.10:g.19959744_19959755delinsCTCACCCTCTAA , CM000684.1:g.19959744_19959755delinsCTCACCCTCTAA GRCh37
NC_000022.9:g.18339744_18339755delinsCTCACCCTCTAA NCBI36
NG_023326.1:g.49555_49566delinsTTAGAGGGTGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000263207.8:c.2695+126_2695+137delinsTTAGAGGGTGAG MANE Select ENSP00000263207.3:n.2695+126_2695+137delinsTTAGAGGGTGAG
ENST00000263207.7:c.2695+126_2695+137delinsTTAGAGGGTGAG ENSP00000263207.3:n.2695+126_2695+137delinsTTAGAGGGTGAG
ENST00000401994.5:c.2506+126_2506+137delinsTTAGAGGGTGAG ENSP00000384341.1:n.2506+126_2506+137delinsTTAGAGGGTGAG
ENST00000406259.1:c.2677+126_2677+137delinsTTAGAGGGTGAG ENSP00000385444.1:n.2677+126_2677+137delinsTTAGAGGGTGAG
ENST00000406522.5:c.2488+126_2488+137delinsTTAGAGGGTGAG ENSP00000384732.1:n.2488+126_2488+137delinsTTAGAGGGTGAG
ENST00000495096.5:n.1617+126_1617+137delinsTTAGAGGGTGAG
NM_001670.2:c.2695+126_2695+137delinsTTAGAGGGTGAG NP_001661.1:n.2695+126_2695+137delinsTTAGAGGGTGAG
XM_005261242.1:c.2677+126_2677+137delinsTTAGAGGGTGAG XP_005261299.1:n.2677+126_2677+137delinsTTAGAGGGTGAG
XM_005261243.3:c.2677+126_2677+137delinsTTAGAGGGTGAG XP_005261300.1:n.2677+126_2677+137delinsTTAGAGGGTGAG
XM_005261244.3:c.2677+126_2677+137delinsTTAGAGGGTGAG XP_005261301.1:n.2677+126_2677+137delinsTTAGAGGGTGAG
XM_006724243.1:c.2695+126_2695+137delinsTTAGAGGGTGAG XP_006724306.1:n.2695+126_2695+137delinsTTAGAGGGTGAG
XM_006724245.2:c.2695+126_2695+137delinsTTAGAGGGTGAG XP_006724308.1:n.2695+126_2695+137delinsTTAGAGGGTGAG
XM_006724246.2:c.2449+126_2449+137delinsTTAGAGGGTGAG XP_006724309.1:n.2449+126_2449+137delinsTTAGAGGGTGAG
XM_006724247.2:c.2506+126_2506+137delinsTTAGAGGGTGAG XP_006724310.1:n.2506+126_2506+137delinsTTAGAGGGTGAG
XM_006724248.2:c.2488+126_2488+137delinsTTAGAGGGTGAG XP_006724311.1:n.2488+126_2488+137delinsTTAGAGGGTGAG
XM_011530179.1:c.2662+126_2662+137delinsTTAGAGGGTGAG XP_011528481.1:n.2662+126_2662+137delinsTTAGAGGGTGAG
XM_011530180.1:c.2695+126_2695+137delinsTTAGAGGGTGAG XP_011528482.1:n.2695+126_2695+137delinsTTAGAGGGTGAG
XM_011530182.1:c.1261+126_1261+137delinsTTAGAGGGTGAG XP_011528484.1:n.1261+126_1261+137delinsTTAGAGGGTGAG
XM_011530183.1:c.1243+126_1243+137delinsTTAGAGGGTGAG XP_011528485.1:n.1243+126_1243+137delinsTTAGAGGGTGAG
XR_937863.1:n.2782+126_2782+137delinsTTAGAGGGTGAG
XR_937864.1:n.2782+126_2782+137delinsTTAGAGGGTGAG
XM_005261242.3:c.2677+126_2677+137delinsTTAGAGGGTGAG XP_005261299.1:n.2677+126_2677+137delinsTTAGAGGGTGAG
XM_005261243.4:c.2677+126_2677+137delinsTTAGAGGGTGAG XP_005261300.1:n.2677+126_2677+137delinsTTAGAGGGTGAG
XM_005261244.4:c.2677+126_2677+137delinsTTAGAGGGTGAG XP_005261301.1:n.2677+126_2677+137delinsTTAGAGGGTGAG
XM_006724243.3:c.2695+126_2695+137delinsTTAGAGGGTGAG XP_006724306.1:n.2695+126_2695+137delinsTTAGAGGGTGAG
XM_006724245.3:c.2695+126_2695+137delinsTTAGAGGGTGAG XP_006724308.1:n.2695+126_2695+137delinsTTAGAGGGTGAG
XM_006724246.4:c.2449+126_2449+137delinsTTAGAGGGTGAG XP_006724309.1:n.2449+126_2449+137delinsTTAGAGGGTGAG
XM_006724247.4:c.2506+126_2506+137delinsTTAGAGGGTGAG XP_006724310.1:n.2506+126_2506+137delinsTTAGAGGGTGAG
XM_006724248.4:c.2488+126_2488+137delinsTTAGAGGGTGAG XP_006724311.1:n.2488+126_2488+137delinsTTAGAGGGTGAG
XM_011530179.3:c.2662+126_2662+137delinsTTAGAGGGTGAG XP_011528481.1:n.2662+126_2662+137delinsTTAGAGGGTGAG
XM_011530182.3:c.1261+126_1261+137delinsTTAGAGGGTGAG XP_011528484.1:n.1261+126_1261+137delinsTTAGAGGGTGAG
XM_011530183.3:c.1243+126_1243+137delinsTTAGAGGGTGAG XP_011528485.1:n.1243+126_1243+137delinsTTAGAGGGTGAG
XM_024452249.1:c.2449+126_2449+137delinsTTAGAGGGTGAG XP_024308017.1:n.2449+126_2449+137delinsTTAGAGGGTGAG
XR_937863.2:n.2782+126_2782+137delinsTTAGAGGGTGAG
NM_001670.3:c.2695+126_2695+137delinsTTAGAGGGTGAG MANE Select NP_001661.1:n.2695+126_2695+137delinsTTAGAGGGTGAG