Canonical Allele Identifier: CA2655341761

Gene: ARVCF

Linked Data

• gnomAD v4: 22-19972278-CCCCATAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972281_19972289del , CM000684.2:g.19972281_19972289del	GRCh38
NC_000022.10:g.19959804_19959812del , CM000684.1:g.19959804_19959812del	GRCh37
NC_000022.9:g.18339804_18339812del	NCBI36
NG_023326.1:g.49500_49508del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2695+71_2695+79del MANE Select	ENSP00000263207.3:n.2695+71_2695+79del
ENST00000263207.7:c.2695+71_2695+79del	ENSP00000263207.3:n.2695+71_2695+79del
ENST00000401994.5:c.2506+71_2506+79del	ENSP00000384341.1:n.2506+71_2506+79del
ENST00000406259.1:c.2677+71_2677+79del	ENSP00000385444.1:n.2677+71_2677+79del
ENST00000406522.5:c.2488+71_2488+79del	ENSP00000384732.1:n.2488+71_2488+79del
ENST00000495096.5:n.1617+71_1617+79del
NM_001670.2:c.2695+71_2695+79del	NP_001661.1:n.2695+71_2695+79del
XM_005261242.1:c.2677+71_2677+79del	XP_005261299.1:n.2677+71_2677+79del
XM_005261243.3:c.2677+71_2677+79del	XP_005261300.1:n.2677+71_2677+79del
XM_005261244.3:c.2677+71_2677+79del	XP_005261301.1:n.2677+71_2677+79del
XM_006724243.1:c.2695+71_2695+79del	XP_006724306.1:n.2695+71_2695+79del
XM_006724245.2:c.2695+71_2695+79del	XP_006724308.1:n.2695+71_2695+79del
XM_006724246.2:c.2449+71_2449+79del	XP_006724309.1:n.2449+71_2449+79del
XM_006724247.2:c.2506+71_2506+79del	XP_006724310.1:n.2506+71_2506+79del
XM_006724248.2:c.2488+71_2488+79del	XP_006724311.1:n.2488+71_2488+79del
XM_011530179.1:c.2662+71_2662+79del	XP_011528481.1:n.2662+71_2662+79del
XM_011530180.1:c.2695+71_2695+79del	XP_011528482.1:n.2695+71_2695+79del
XM_011530182.1:c.1261+71_1261+79del	XP_011528484.1:n.1261+71_1261+79del
XM_011530183.1:c.1243+71_1243+79del	XP_011528485.1:n.1243+71_1243+79del
XR_937863.1:n.2782+71_2782+79del
XR_937864.1:n.2782+71_2782+79del
XM_005261242.3:c.2677+71_2677+79del	XP_005261299.1:n.2677+71_2677+79del
XM_005261243.4:c.2677+71_2677+79del	XP_005261300.1:n.2677+71_2677+79del
XM_005261244.4:c.2677+71_2677+79del	XP_005261301.1:n.2677+71_2677+79del
XM_006724243.3:c.2695+71_2695+79del	XP_006724306.1:n.2695+71_2695+79del
XM_006724245.3:c.2695+71_2695+79del	XP_006724308.1:n.2695+71_2695+79del
XM_006724246.4:c.2449+71_2449+79del	XP_006724309.1:n.2449+71_2449+79del
XM_006724247.4:c.2506+71_2506+79del	XP_006724310.1:n.2506+71_2506+79del
XM_006724248.4:c.2488+71_2488+79del	XP_006724311.1:n.2488+71_2488+79del
XM_011530179.3:c.2662+71_2662+79del	XP_011528481.1:n.2662+71_2662+79del
XM_011530182.3:c.1261+71_1261+79del	XP_011528484.1:n.1261+71_1261+79del
XM_011530183.3:c.1243+71_1243+79del	XP_011528485.1:n.1243+71_1243+79del
XM_024452249.1:c.2449+71_2449+79del	XP_024308017.1:n.2449+71_2449+79del
XR_937863.2:n.2782+71_2782+79del
NM_001670.3:c.2695+71_2695+79del MANE Select	NP_001661.1:n.2695+71_2695+79del