Canonical Allele Identifier: CA2396130935

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972989_19972991delinsACT , CM000684.2:g.19972989_19972991delinsACT	GRCh38
NC_000022.10:g.19960512_19960514delinsACT , CM000684.1:g.19960512_19960514delinsACT	GRCh37
NC_000022.9:g.18340512_18340514delinsACT	NCBI36
NG_023326.1:g.48796_48798delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2484_2486delinsAGT MANE Select	ENSP00000263207.3:p.Thr828=
ENST00000263207.7:c.2484_2486delinsAGT	ENSP00000263207.3:p.Thr828=
ENST00000401994.5:c.2295_2297delinsAGT	ENSP00000384341.1:p.Thr765=
ENST00000406259.1:c.2466_2468delinsAGT	ENSP00000385444.1:p.Thr822=
ENST00000406522.5:c.2277_2279delinsAGT	ENSP00000384732.1:p.Thr759=
ENST00000495096.5:n.1406_1408delinsAGT
NM_001670.2:c.2484_2486delinsAGT	NP_001661.1:p.Thr828=
XM_005261242.1:c.2466_2468delinsAGT	XP_005261299.1:p.Thr822=
XM_005261243.3:c.2466_2468delinsAGT	XP_005261300.1:p.Thr822=
XM_005261244.3:c.2466_2468delinsAGT	XP_005261301.1:p.Thr822=
XM_006724243.1:c.2484_2486delinsAGT	XP_006724306.1:p.Thr828=
XM_006724245.2:c.2484_2486delinsAGT	XP_006724308.1:p.Thr828=
XM_006724246.2:c.2238_2240delinsAGT	XP_006724309.1:p.Thr746=
XM_006724247.2:c.2295_2297delinsAGT	XP_006724310.1:p.Thr765=
XM_006724248.2:c.2277_2279delinsAGT	XP_006724311.1:p.Thr759=
XM_011530179.1:c.2451_2453delinsAGT	XP_011528481.1:p.Thr817=
XM_011530180.1:c.2484_2486delinsAGT	XP_011528482.1:p.Thr828=
XM_011530182.1:c.1050_1052delinsAGT	XP_011528484.1:p.Thr350=
XM_011530183.1:c.1032_1034delinsAGT	XP_011528485.1:p.Thr344=
XR_937863.1:n.2571_2573delinsAGT
XR_937864.1:n.2571_2573delinsAGT
XM_005261242.3:c.2466_2468delinsAGT	XP_005261299.1:p.Thr822=
XM_005261243.4:c.2466_2468delinsAGT	XP_005261300.1:p.Thr822=
XM_005261244.4:c.2466_2468delinsAGT	XP_005261301.1:p.Thr822=
XM_006724243.3:c.2484_2486delinsAGT	XP_006724306.1:p.Thr828=
XM_006724245.3:c.2484_2486delinsAGT	XP_006724308.1:p.Thr828=
XM_006724246.4:c.2238_2240delinsAGT	XP_006724309.1:p.Thr746=
XM_006724247.4:c.2295_2297delinsAGT	XP_006724310.1:p.Thr765=
XM_006724248.4:c.2277_2279delinsAGT	XP_006724311.1:p.Thr759=
XM_011530179.3:c.2451_2453delinsAGT	XP_011528481.1:p.Thr817=
XM_011530182.3:c.1050_1052delinsAGT	XP_011528484.1:p.Thr350=
XM_011530183.3:c.1032_1034delinsAGT	XP_011528485.1:p.Thr344=
XM_024452249.1:c.2238_2240delinsAGT	XP_024308017.1:p.Thr746=
XR_937863.2:n.2571_2573delinsAGT
NM_001670.3:c.2484_2486delinsAGT MANE Select	NP_001661.1:p.Thr828=