Canonical Allele Identifier: CA2396130718

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972651_19972654delinsACTC , CM000684.2:g.19972651_19972654delinsACTC	GRCh38
NC_000022.10:g.19960174_19960177delinsACTC , CM000684.1:g.19960174_19960177delinsACTC	GRCh37
NC_000022.9:g.18340174_18340177delinsACTC	NCBI36
NG_023326.1:g.49133_49136delinsGAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2641+83_2641+86delinsGAGT MANE Select	ENSP00000263207.3:n.2641+83_2641+86delinsGAGT
ENST00000263207.7:c.2641+83_2641+86delinsGAGT	ENSP00000263207.3:n.2641+83_2641+86delinsGAGT
ENST00000401994.5:c.2452+83_2452+86delinsGAGT	ENSP00000384341.1:n.2452+83_2452+86delinsGAGT
ENST00000406259.1:c.2623+83_2623+86delinsGAGT	ENSP00000385444.1:n.2623+83_2623+86delinsGAGT
ENST00000406522.5:c.2434+83_2434+86delinsGAGT	ENSP00000384732.1:n.2434+83_2434+86delinsGAGT
ENST00000495096.5:n.1563+83_1563+86delinsGAGT
NM_001670.2:c.2641+83_2641+86delinsGAGT	NP_001661.1:n.2641+83_2641+86delinsGAGT
XM_005261242.1:c.2623+83_2623+86delinsGAGT	XP_005261299.1:n.2623+83_2623+86delinsGAGT
XM_005261243.3:c.2623+83_2623+86delinsGAGT	XP_005261300.1:n.2623+83_2623+86delinsGAGT
XM_005261244.3:c.2623+83_2623+86delinsGAGT	XP_005261301.1:n.2623+83_2623+86delinsGAGT
XM_006724243.1:c.2641+83_2641+86delinsGAGT	XP_006724306.1:n.2641+83_2641+86delinsGAGT
XM_006724245.2:c.2641+83_2641+86delinsGAGT	XP_006724308.1:n.2641+83_2641+86delinsGAGT
XM_006724246.2:c.2395+83_2395+86delinsGAGT	XP_006724309.1:n.2395+83_2395+86delinsGAGT
XM_006724247.2:c.2452+83_2452+86delinsGAGT	XP_006724310.1:n.2452+83_2452+86delinsGAGT
XM_006724248.2:c.2434+83_2434+86delinsGAGT	XP_006724311.1:n.2434+83_2434+86delinsGAGT
XM_011530179.1:c.2608+83_2608+86delinsGAGT	XP_011528481.1:n.2608+83_2608+86delinsGAGT
XM_011530180.1:c.2641+83_2641+86delinsGAGT	XP_011528482.1:n.2641+83_2641+86delinsGAGT
XM_011530182.1:c.1207+83_1207+86delinsGAGT	XP_011528484.1:n.1207+83_1207+86delinsGAGT
XM_011530183.1:c.1189+83_1189+86delinsGAGT	XP_011528485.1:n.1189+83_1189+86delinsGAGT
XR_937863.1:n.2728+83_2728+86delinsGAGT
XR_937864.1:n.2728+83_2728+86delinsGAGT
XM_005261242.3:c.2623+83_2623+86delinsGAGT	XP_005261299.1:n.2623+83_2623+86delinsGAGT
XM_005261243.4:c.2623+83_2623+86delinsGAGT	XP_005261300.1:n.2623+83_2623+86delinsGAGT
XM_005261244.4:c.2623+83_2623+86delinsGAGT	XP_005261301.1:n.2623+83_2623+86delinsGAGT
XM_006724243.3:c.2641+83_2641+86delinsGAGT	XP_006724306.1:n.2641+83_2641+86delinsGAGT
XM_006724245.3:c.2641+83_2641+86delinsGAGT	XP_006724308.1:n.2641+83_2641+86delinsGAGT
XM_006724246.4:c.2395+83_2395+86delinsGAGT	XP_006724309.1:n.2395+83_2395+86delinsGAGT
XM_006724247.4:c.2452+83_2452+86delinsGAGT	XP_006724310.1:n.2452+83_2452+86delinsGAGT
XM_006724248.4:c.2434+83_2434+86delinsGAGT	XP_006724311.1:n.2434+83_2434+86delinsGAGT
XM_011530179.3:c.2608+83_2608+86delinsGAGT	XP_011528481.1:n.2608+83_2608+86delinsGAGT
XM_011530182.3:c.1207+83_1207+86delinsGAGT	XP_011528484.1:n.1207+83_1207+86delinsGAGT
XM_011530183.3:c.1189+83_1189+86delinsGAGT	XP_011528485.1:n.1189+83_1189+86delinsGAGT
XM_024452249.1:c.2395+83_2395+86delinsGAGT	XP_024308017.1:n.2395+83_2395+86delinsGAGT
XR_937863.2:n.2728+83_2728+86delinsGAGT
NM_001670.3:c.2641+83_2641+86delinsGAGT MANE Select	NP_001661.1:n.2641+83_2641+86delinsGAGT