Canonical Allele Identifier: CA2396130836

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972849_19972851delinsCAG , CM000684.2:g.19972849_19972851delinsCAG	GRCh38
NC_000022.10:g.19960372_19960374delinsCAG , CM000684.1:g.19960372_19960374delinsCAG	GRCh37
NC_000022.9:g.18340372_18340374delinsCAG	NCBI36
NG_023326.1:g.48936_48938delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2551-24_2551-22delinsCTG MANE Select	ENSP00000263207.3:n.2551-24_2551-22delinsCTG
ENST00000263207.7:c.2551-24_2551-22delinsCTG	ENSP00000263207.3:n.2551-24_2551-22delinsCTG
ENST00000401994.5:c.2362-24_2362-22delinsCTG	ENSP00000384341.1:n.2362-24_2362-22delinsCTG
ENST00000406259.1:c.2533-24_2533-22delinsCTG	ENSP00000385444.1:n.2533-24_2533-22delinsCTG
ENST00000406522.5:c.2344-24_2344-22delinsCTG	ENSP00000384732.1:n.2344-24_2344-22delinsCTG
ENST00000495096.5:n.1473-24_1473-22delinsCTG
NM_001670.2:c.2551-24_2551-22delinsCTG	NP_001661.1:n.2551-24_2551-22delinsCTG
XM_005261242.1:c.2533-24_2533-22delinsCTG	XP_005261299.1:n.2533-24_2533-22delinsCTG
XM_005261243.3:c.2533-24_2533-22delinsCTG	XP_005261300.1:n.2533-24_2533-22delinsCTG
XM_005261244.3:c.2533-24_2533-22delinsCTG	XP_005261301.1:n.2533-24_2533-22delinsCTG
XM_006724243.1:c.2551-24_2551-22delinsCTG	XP_006724306.1:n.2551-24_2551-22delinsCTG
XM_006724245.2:c.2551-24_2551-22delinsCTG	XP_006724308.1:n.2551-24_2551-22delinsCTG
XM_006724246.2:c.2305-24_2305-22delinsCTG	XP_006724309.1:n.2305-24_2305-22delinsCTG
XM_006724247.2:c.2362-24_2362-22delinsCTG	XP_006724310.1:n.2362-24_2362-22delinsCTG
XM_006724248.2:c.2344-24_2344-22delinsCTG	XP_006724311.1:n.2344-24_2344-22delinsCTG
XM_011530179.1:c.2518-24_2518-22delinsCTG	XP_011528481.1:n.2518-24_2518-22delinsCTG
XM_011530180.1:c.2551-24_2551-22delinsCTG	XP_011528482.1:n.2551-24_2551-22delinsCTG
XM_011530182.1:c.1117-24_1117-22delinsCTG	XP_011528484.1:n.1117-24_1117-22delinsCTG
XM_011530183.1:c.1099-24_1099-22delinsCTG	XP_011528485.1:n.1099-24_1099-22delinsCTG
XR_937863.1:n.2638-24_2638-22delinsCTG
XR_937864.1:n.2638-24_2638-22delinsCTG
XM_005261242.3:c.2533-24_2533-22delinsCTG	XP_005261299.1:n.2533-24_2533-22delinsCTG
XM_005261243.4:c.2533-24_2533-22delinsCTG	XP_005261300.1:n.2533-24_2533-22delinsCTG
XM_005261244.4:c.2533-24_2533-22delinsCTG	XP_005261301.1:n.2533-24_2533-22delinsCTG
XM_006724243.3:c.2551-24_2551-22delinsCTG	XP_006724306.1:n.2551-24_2551-22delinsCTG
XM_006724245.3:c.2551-24_2551-22delinsCTG	XP_006724308.1:n.2551-24_2551-22delinsCTG
XM_006724246.4:c.2305-24_2305-22delinsCTG	XP_006724309.1:n.2305-24_2305-22delinsCTG
XM_006724247.4:c.2362-24_2362-22delinsCTG	XP_006724310.1:n.2362-24_2362-22delinsCTG
XM_006724248.4:c.2344-24_2344-22delinsCTG	XP_006724311.1:n.2344-24_2344-22delinsCTG
XM_011530179.3:c.2518-24_2518-22delinsCTG	XP_011528481.1:n.2518-24_2518-22delinsCTG
XM_011530182.3:c.1117-24_1117-22delinsCTG	XP_011528484.1:n.1117-24_1117-22delinsCTG
XM_011530183.3:c.1099-24_1099-22delinsCTG	XP_011528485.1:n.1099-24_1099-22delinsCTG
XM_024452249.1:c.2305-24_2305-22delinsCTG	XP_024308017.1:n.2305-24_2305-22delinsCTG
XR_937863.2:n.2638-24_2638-22delinsCTG
NM_001670.3:c.2551-24_2551-22delinsCTG MANE Select	NP_001661.1:n.2551-24_2551-22delinsCTG