Canonical Allele Identifier: CA2655342621

Gene: ARVCF

Linked Data

• gnomAD v4: 22-19972945-AACCATCTTTCTGCAAGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972950_19972967del , CM000684.2:g.19972950_19972967del	GRCh38
NC_000022.10:g.19960473_19960490del , CM000684.1:g.19960473_19960490del	GRCh37
NC_000022.9:g.18340473_18340490del	NCBI36
NG_023326.1:g.48824_48841del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2512_2529del MANE Select	ENSP00000263207.3:p.Thr838_Gly843del
ENST00000263207.7:c.2512_2529del	ENSP00000263207.3:p.Thr838_Gly843del
ENST00000401994.5:c.2323_2340del	ENSP00000384341.1:p.Thr775_Gly780del
ENST00000406259.1:c.2494_2511del	ENSP00000385444.1:p.Thr832_Gly837del
ENST00000406522.5:c.2305_2322del	ENSP00000384732.1:p.Thr769_Gly774del
ENST00000495096.5:n.1434_1451del
NM_001670.2:c.2512_2529del	NP_001661.1:p.Thr838_Gly843del
XM_005261242.1:c.2494_2511del	XP_005261299.1:p.Thr832_Gly837del
XM_005261243.3:c.2494_2511del	XP_005261300.1:p.Thr832_Gly837del
XM_005261244.3:c.2494_2511del	XP_005261301.1:p.Thr832_Gly837del
XM_006724243.1:c.2512_2529del	XP_006724306.1:p.Thr838_Gly843del
XM_006724245.2:c.2512_2529del	XP_006724308.1:p.Thr838_Gly843del
XM_006724246.2:c.2266_2283del	XP_006724309.1:p.Thr756_Gly761del
XM_006724247.2:c.2323_2340del	XP_006724310.1:p.Thr775_Gly780del
XM_006724248.2:c.2305_2322del	XP_006724311.1:p.Thr769_Gly774del
XM_011530179.1:c.2479_2496del	XP_011528481.1:p.Thr827_Gly832del
XM_011530180.1:c.2512_2529del	XP_011528482.1:p.Thr838_Gly843del
XM_011530182.1:c.1078_1095del	XP_011528484.1:p.Thr360_Gly365del
XM_011530183.1:c.1060_1077del	XP_011528485.1:p.Thr354_Gly359del
XR_937863.1:n.2599_2616del
XR_937864.1:n.2599_2616del
XM_005261242.3:c.2494_2511del	XP_005261299.1:p.Thr832_Gly837del
XM_005261243.4:c.2494_2511del	XP_005261300.1:p.Thr832_Gly837del
XM_005261244.4:c.2494_2511del	XP_005261301.1:p.Thr832_Gly837del
XM_006724243.3:c.2512_2529del	XP_006724306.1:p.Thr838_Gly843del
XM_006724245.3:c.2512_2529del	XP_006724308.1:p.Thr838_Gly843del
XM_006724246.4:c.2266_2283del	XP_006724309.1:p.Thr756_Gly761del
XM_006724247.4:c.2323_2340del	XP_006724310.1:p.Thr775_Gly780del
XM_006724248.4:c.2305_2322del	XP_006724311.1:p.Thr769_Gly774del
XM_011530179.3:c.2479_2496del	XP_011528481.1:p.Thr827_Gly832del
XM_011530182.3:c.1078_1095del	XP_011528484.1:p.Thr360_Gly365del
XM_011530183.3:c.1060_1077del	XP_011528485.1:p.Thr354_Gly359del
XM_024452249.1:c.2266_2283del	XP_024308017.1:p.Thr756_Gly761del
XR_937863.2:n.2599_2616del
NM_001670.3:c.2512_2529del MANE Select	NP_001661.1:p.Thr838_Gly843del