Canonical Allele Identifier: CA2396130872

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972896_19972897delinsGA , CM000684.2:g.19972896_19972897delinsGA	GRCh38
NC_000022.10:g.19960419_19960420delinsGA , CM000684.1:g.19960419_19960420delinsGA	GRCh37
NC_000022.9:g.18340419_18340420delinsGA	NCBI36
NG_023326.1:g.48890_48891delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2550+28_2550+29delinsTC MANE Select	ENSP00000263207.3:n.2550+28_2550+29delinsTC
ENST00000263207.7:c.2550+28_2550+29delinsTC	ENSP00000263207.3:n.2550+28_2550+29delinsTC
ENST00000401994.5:c.2361+28_2361+29delinsTC	ENSP00000384341.1:n.2361+28_2361+29delinsTC
ENST00000406259.1:c.2532+28_2532+29delinsTC	ENSP00000385444.1:n.2532+28_2532+29delinsTC
ENST00000406522.5:c.2343+28_2343+29delinsTC	ENSP00000384732.1:n.2343+28_2343+29delinsTC
ENST00000495096.5:n.1472+28_1472+29delinsTC
NM_001670.2:c.2550+28_2550+29delinsTC	NP_001661.1:n.2550+28_2550+29delinsTC
XM_005261242.1:c.2532+28_2532+29delinsTC	XP_005261299.1:n.2532+28_2532+29delinsTC
XM_005261243.3:c.2532+28_2532+29delinsTC	XP_005261300.1:n.2532+28_2532+29delinsTC
XM_005261244.3:c.2532+28_2532+29delinsTC	XP_005261301.1:n.2532+28_2532+29delinsTC
XM_006724243.1:c.2550+28_2550+29delinsTC	XP_006724306.1:n.2550+28_2550+29delinsTC
XM_006724245.2:c.2550+28_2550+29delinsTC	XP_006724308.1:n.2550+28_2550+29delinsTC
XM_006724246.2:c.2304+28_2304+29delinsTC	XP_006724309.1:n.2304+28_2304+29delinsTC
XM_006724247.2:c.2361+28_2361+29delinsTC	XP_006724310.1:n.2361+28_2361+29delinsTC
XM_006724248.2:c.2343+28_2343+29delinsTC	XP_006724311.1:n.2343+28_2343+29delinsTC
XM_011530179.1:c.2517+28_2517+29delinsTC	XP_011528481.1:n.2517+28_2517+29delinsTC
XM_011530180.1:c.2550+28_2550+29delinsTC	XP_011528482.1:n.2550+28_2550+29delinsTC
XM_011530182.1:c.1116+28_1116+29delinsTC	XP_011528484.1:n.1116+28_1116+29delinsTC
XM_011530183.1:c.1098+28_1098+29delinsTC	XP_011528485.1:n.1098+28_1098+29delinsTC
XR_937863.1:n.2637+28_2637+29delinsTC
XR_937864.1:n.2637+28_2637+29delinsTC
XM_005261242.3:c.2532+28_2532+29delinsTC	XP_005261299.1:n.2532+28_2532+29delinsTC
XM_005261243.4:c.2532+28_2532+29delinsTC	XP_005261300.1:n.2532+28_2532+29delinsTC
XM_005261244.4:c.2532+28_2532+29delinsTC	XP_005261301.1:n.2532+28_2532+29delinsTC
XM_006724243.3:c.2550+28_2550+29delinsTC	XP_006724306.1:n.2550+28_2550+29delinsTC
XM_006724245.3:c.2550+28_2550+29delinsTC	XP_006724308.1:n.2550+28_2550+29delinsTC
XM_006724246.4:c.2304+28_2304+29delinsTC	XP_006724309.1:n.2304+28_2304+29delinsTC
XM_006724247.4:c.2361+28_2361+29delinsTC	XP_006724310.1:n.2361+28_2361+29delinsTC
XM_006724248.4:c.2343+28_2343+29delinsTC	XP_006724311.1:n.2343+28_2343+29delinsTC
XM_011530179.3:c.2517+28_2517+29delinsTC	XP_011528481.1:n.2517+28_2517+29delinsTC
XM_011530182.3:c.1116+28_1116+29delinsTC	XP_011528484.1:n.1116+28_1116+29delinsTC
XM_011530183.3:c.1098+28_1098+29delinsTC	XP_011528485.1:n.1098+28_1098+29delinsTC
XM_024452249.1:c.2304+28_2304+29delinsTC	XP_024308017.1:n.2304+28_2304+29delinsTC
XR_937863.2:n.2637+28_2637+29delinsTC
NM_001670.3:c.2550+28_2550+29delinsTC MANE Select	NP_001661.1:n.2550+28_2550+29delinsTC