Canonical Allele Identifier: CA2655342142
Gene: ARVCF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19972548_19972566dup , CM000684.2:g.19972548_19972566dup GRCh38
NC_000022.10:g.19960071_19960089dup , CM000684.1:g.19960071_19960089dup GRCh37
NC_000022.9:g.18340071_18340089dup NCBI36
NG_023326.1:g.49222_49240dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000263207.8:c.2642-154_2642-136dup MANE Select ENSP00000263207.3:n.2642-154_2642-136dup
ENST00000263207.7:c.2642-154_2642-136dup ENSP00000263207.3:n.2642-154_2642-136dup
ENST00000401994.5:c.2453-154_2453-136dup ENSP00000384341.1:n.2453-154_2453-136dup
ENST00000406259.1:c.2624-154_2624-136dup ENSP00000385444.1:n.2624-154_2624-136dup
ENST00000406522.5:c.2435-154_2435-136dup ENSP00000384732.1:n.2435-154_2435-136dup
ENST00000495096.5:n.1564-154_1564-136dup
NM_001670.2:c.2642-154_2642-136dup NP_001661.1:n.2642-154_2642-136dup
XM_005261242.1:c.2624-154_2624-136dup XP_005261299.1:n.2624-154_2624-136dup
XM_005261243.3:c.2624-154_2624-136dup XP_005261300.1:n.2624-154_2624-136dup
XM_005261244.3:c.2624-154_2624-136dup XP_005261301.1:n.2624-154_2624-136dup
XM_006724243.1:c.2642-154_2642-136dup XP_006724306.1:n.2642-154_2642-136dup
XM_006724245.2:c.2642-154_2642-136dup XP_006724308.1:n.2642-154_2642-136dup
XM_006724246.2:c.2396-154_2396-136dup XP_006724309.1:n.2396-154_2396-136dup
XM_006724247.2:c.2453-154_2453-136dup XP_006724310.1:n.2453-154_2453-136dup
XM_006724248.2:c.2435-154_2435-136dup XP_006724311.1:n.2435-154_2435-136dup
XM_011530179.1:c.2609-154_2609-136dup XP_011528481.1:n.2609-154_2609-136dup
XM_011530180.1:c.2642-154_2642-136dup XP_011528482.1:n.2642-154_2642-136dup
XM_011530182.1:c.1208-154_1208-136dup XP_011528484.1:n.1208-154_1208-136dup
XM_011530183.1:c.1190-154_1190-136dup XP_011528485.1:n.1190-154_1190-136dup
XR_937863.1:n.2729-154_2729-136dup
XR_937864.1:n.2729-154_2729-136dup
XM_005261242.3:c.2624-154_2624-136dup XP_005261299.1:n.2624-154_2624-136dup
XM_005261243.4:c.2624-154_2624-136dup XP_005261300.1:n.2624-154_2624-136dup
XM_005261244.4:c.2624-154_2624-136dup XP_005261301.1:n.2624-154_2624-136dup
XM_006724243.3:c.2642-154_2642-136dup XP_006724306.1:n.2642-154_2642-136dup
XM_006724245.3:c.2642-154_2642-136dup XP_006724308.1:n.2642-154_2642-136dup
XM_006724246.4:c.2396-154_2396-136dup XP_006724309.1:n.2396-154_2396-136dup
XM_006724247.4:c.2453-154_2453-136dup XP_006724310.1:n.2453-154_2453-136dup
XM_006724248.4:c.2435-154_2435-136dup XP_006724311.1:n.2435-154_2435-136dup
XM_011530179.3:c.2609-154_2609-136dup XP_011528481.1:n.2609-154_2609-136dup
XM_011530182.3:c.1208-154_1208-136dup XP_011528484.1:n.1208-154_1208-136dup
XM_011530183.3:c.1190-154_1190-136dup XP_011528485.1:n.1190-154_1190-136dup
XM_024452249.1:c.2396-154_2396-136dup XP_024308017.1:n.2396-154_2396-136dup
XR_937863.2:n.2729-154_2729-136dup
NM_001670.3:c.2642-154_2642-136dup MANE Select NP_001661.1:n.2642-154_2642-136dup