Canonical Allele Identifier: CA2396130529

Gene: ARVCF

Linked Data

• dbSNP Id: rs1942858907

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972340_19972375del , CM000684.2:g.19972340_19972375del	GRCh38
NC_000022.10:g.19959863_19959898del , CM000684.1:g.19959863_19959898del	GRCh37
NC_000022.9:g.18339863_18339898del	NCBI36
NG_023326.1:g.49415_49450del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2681_2695+21del
ENST00000263207.7:c.2681_2695+21del
ENST00000401994.5:c.2492_2506+21del
ENST00000406259.1:c.2663_2677+21del
ENST00000406522.5:c.2474_2488+21del
ENST00000495096.5:n.1603_1617+21del
NM_001670.2:c.2681_2695+21del
XM_005261242.1:c.2663_2677+21del
XM_005261243.3:c.2663_2677+21del
XM_005261244.3:c.2663_2677+21del
XM_006724243.1:c.2681_2695+21del
XM_006724245.2:c.2681_2695+21del
XM_006724246.2:c.2435_2449+21del
XM_006724247.2:c.2492_2506+21del
XM_006724248.2:c.2474_2488+21del
XM_011530179.1:c.2648_2662+21del
XM_011530180.1:c.2681_2695+21del
XM_011530182.1:c.1247_1261+21del
XM_011530183.1:c.1229_1243+21del
XR_937863.1:n.2768_2782+21del
XR_937864.1:n.2768_2782+21del
XM_005261242.3:c.2663_2677+21del
XM_005261243.4:c.2663_2677+21del
XM_005261244.4:c.2663_2677+21del
XM_006724243.3:c.2681_2695+21del
XM_006724245.3:c.2681_2695+21del
XM_006724246.4:c.2435_2449+21del
XM_006724247.4:c.2492_2506+21del
XM_006724248.4:c.2474_2488+21del
XM_011530179.3:c.2648_2662+21del
XM_011530182.3:c.1247_1261+21del
XM_011530183.3:c.1229_1243+21del
XM_024452249.1:c.2435_2449+21del
XR_937863.2:n.2768_2782+21del
NM_001670.3:c.2681_2695+21del