Canonical Allele Identifier: CA1024139682

Gene: ARVCF

Linked Data

• gnomAD v3: 22-19972251-TCTCTCCTCC-T
• gnomAD v4: 22-19972251-TCTCTCCTCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972252_19972260del , CM000684.2:g.19972252_19972260del	GRCh38
NC_000022.10:g.19959775_19959783del , CM000684.1:g.19959775_19959783del	GRCh37
NC_000022.9:g.18339775_18339783del	NCBI36
NG_023326.1:g.49527_49535del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2695+98_2695+106del MANE Select	ENSP00000263207.3:n.2695+98_2695+106del
ENST00000263207.7:c.2695+98_2695+106del	ENSP00000263207.3:n.2695+98_2695+106del
ENST00000401994.5:c.2506+98_2506+106del	ENSP00000384341.1:n.2506+98_2506+106del
ENST00000406259.1:c.2677+98_2677+106del	ENSP00000385444.1:n.2677+98_2677+106del
ENST00000406522.5:c.2488+98_2488+106del	ENSP00000384732.1:n.2488+98_2488+106del
ENST00000495096.5:n.1617+98_1617+106del
NM_001670.2:c.2695+98_2695+106del	NP_001661.1:n.2695+98_2695+106del
XM_005261242.1:c.2677+98_2677+106del	XP_005261299.1:n.2677+98_2677+106del
XM_005261243.3:c.2677+98_2677+106del	XP_005261300.1:n.2677+98_2677+106del
XM_005261244.3:c.2677+98_2677+106del	XP_005261301.1:n.2677+98_2677+106del
XM_006724243.1:c.2695+98_2695+106del	XP_006724306.1:n.2695+98_2695+106del
XM_006724245.2:c.2695+98_2695+106del	XP_006724308.1:n.2695+98_2695+106del
XM_006724246.2:c.2449+98_2449+106del	XP_006724309.1:n.2449+98_2449+106del
XM_006724247.2:c.2506+98_2506+106del	XP_006724310.1:n.2506+98_2506+106del
XM_006724248.2:c.2488+98_2488+106del	XP_006724311.1:n.2488+98_2488+106del
XM_011530179.1:c.2662+98_2662+106del	XP_011528481.1:n.2662+98_2662+106del
XM_011530180.1:c.2695+98_2695+106del	XP_011528482.1:n.2695+98_2695+106del
XM_011530182.1:c.1261+98_1261+106del	XP_011528484.1:n.1261+98_1261+106del
XM_011530183.1:c.1243+98_1243+106del	XP_011528485.1:n.1243+98_1243+106del
XR_937863.1:n.2782+98_2782+106del
XR_937864.1:n.2782+98_2782+106del
XM_005261242.3:c.2677+98_2677+106del	XP_005261299.1:n.2677+98_2677+106del
XM_005261243.4:c.2677+98_2677+106del	XP_005261300.1:n.2677+98_2677+106del
XM_005261244.4:c.2677+98_2677+106del	XP_005261301.1:n.2677+98_2677+106del
XM_006724243.3:c.2695+98_2695+106del	XP_006724306.1:n.2695+98_2695+106del
XM_006724245.3:c.2695+98_2695+106del	XP_006724308.1:n.2695+98_2695+106del
XM_006724246.4:c.2449+98_2449+106del	XP_006724309.1:n.2449+98_2449+106del
XM_006724247.4:c.2506+98_2506+106del	XP_006724310.1:n.2506+98_2506+106del
XM_006724248.4:c.2488+98_2488+106del	XP_006724311.1:n.2488+98_2488+106del
XM_011530179.3:c.2662+98_2662+106del	XP_011528481.1:n.2662+98_2662+106del
XM_011530182.3:c.1261+98_1261+106del	XP_011528484.1:n.1261+98_1261+106del
XM_011530183.3:c.1243+98_1243+106del	XP_011528485.1:n.1243+98_1243+106del
XM_024452249.1:c.2449+98_2449+106del	XP_024308017.1:n.2449+98_2449+106del
XR_937863.2:n.2782+98_2782+106del
NM_001670.3:c.2695+98_2695+106del MANE Select	NP_001661.1:n.2695+98_2695+106del