Canonical Allele Identifier: CA2655341546

Gene: ARVCF

Linked Data

• gnomAD v4: 22-19972116-G-GA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972116_19972117insA , CM000684.2:g.19972116_19972117insA	GRCh38
NC_000022.10:g.19959639_19959640insA , CM000684.1:g.19959639_19959640insA	GRCh37
NC_000022.9:g.18339639_18339640insA	NCBI36
NG_023326.1:g.49670_49671insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2696-146_2696-145insT MANE Select	ENSP00000263207.3:n.2696-146_2696-145insT
ENST00000263207.7:c.2696-146_2696-145insT	ENSP00000263207.3:n.2696-146_2696-145insT
ENST00000401994.5:c.2507-146_2507-145insT	ENSP00000384341.1:n.2507-146_2507-145insT
ENST00000406259.1:c.2678-146_2678-145insT	ENSP00000385444.1:n.2678-146_2678-145insT
ENST00000406522.5:c.2489-146_2489-145insT	ENSP00000384732.1:n.2489-146_2489-145insT
ENST00000495096.5:n.1618-146_1618-145insT
NM_001670.2:c.2696-146_2696-145insT	NP_001661.1:n.2696-146_2696-145insT
XM_005261242.1:c.2678-146_2678-145insT	XP_005261299.1:n.2678-146_2678-145insT
XM_005261243.3:c.2678-146_2678-145insT	XP_005261300.1:n.2678-146_2678-145insT
XM_005261244.3:c.2678-146_2678-145insT	XP_005261301.1:n.2678-146_2678-145insT
XM_006724243.1:c.2696-146_2696-145insT	XP_006724306.1:n.2696-146_2696-145insT
XM_006724245.2:c.2696-146_2696-145insT	XP_006724308.1:n.2696-146_2696-145insT
XM_006724246.2:c.2450-146_2450-145insT	XP_006724309.1:n.2450-146_2450-145insT
XM_006724247.2:c.2507-146_2507-145insT	XP_006724310.1:n.2507-146_2507-145insT
XM_006724248.2:c.2489-146_2489-145insT	XP_006724311.1:n.2489-146_2489-145insT
XM_011530179.1:c.2663-146_2663-145insT	XP_011528481.1:n.2663-146_2663-145insT
XM_011530180.1:c.2696-146_2696-145insT	XP_011528482.1:n.2696-146_2696-145insT
XM_011530182.1:c.1262-146_1262-145insT	XP_011528484.1:n.1262-146_1262-145insT
XM_011530183.1:c.1244-146_1244-145insT	XP_011528485.1:n.1244-146_1244-145insT
XR_937863.1:n.2783-146_2783-145insT
XR_937864.1:n.2783-146_2783-145insT
XM_005261242.3:c.2678-146_2678-145insT	XP_005261299.1:n.2678-146_2678-145insT
XM_005261243.4:c.2678-146_2678-145insT	XP_005261300.1:n.2678-146_2678-145insT
XM_005261244.4:c.2678-146_2678-145insT	XP_005261301.1:n.2678-146_2678-145insT
XM_006724243.3:c.2696-146_2696-145insT	XP_006724306.1:n.2696-146_2696-145insT
XM_006724245.3:c.2696-146_2696-145insT	XP_006724308.1:n.2696-146_2696-145insT
XM_006724246.4:c.2450-146_2450-145insT	XP_006724309.1:n.2450-146_2450-145insT
XM_006724247.4:c.2507-146_2507-145insT	XP_006724310.1:n.2507-146_2507-145insT
XM_006724248.4:c.2489-146_2489-145insT	XP_006724311.1:n.2489-146_2489-145insT
XM_011530179.3:c.2663-146_2663-145insT	XP_011528481.1:n.2663-146_2663-145insT
XM_011530182.3:c.1262-146_1262-145insT	XP_011528484.1:n.1262-146_1262-145insT
XM_011530183.3:c.1244-146_1244-145insT	XP_011528485.1:n.1244-146_1244-145insT
XM_024452249.1:c.2450-146_2450-145insT	XP_024308017.1:n.2450-146_2450-145insT
XR_937863.2:n.2783-146_2783-145insT
NM_001670.3:c.2696-146_2696-145insT MANE Select	NP_001661.1:n.2696-146_2696-145insT