Canonical Allele Identifier: CA751487134

Gene: ARVCF

Linked Data

• dbSNP Id: rs1364152693
• MyVariant Identifiers: chr22:g.19959943_19959944insAGGAGG (hg19) ; chr22:g.19972420_19972421insAGGAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972426_19972431dup , CM000684.2:g.19972426_19972431dup	GRCh38
NC_000022.10:g.19959949_19959954dup , CM000684.1:g.19959949_19959954dup	GRCh37
NC_000022.9:g.18339949_18339954dup	NCBI36
NG_023326.1:g.49361_49366dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2642-15_2642-10dup MANE Select	ENSP00000263207.3:n.2642-15_2642-10dup
ENST00000263207.7:c.2642-15_2642-10dup	ENSP00000263207.3:n.2642-15_2642-10dup
ENST00000401994.5:c.2453-15_2453-10dup	ENSP00000384341.1:n.2453-15_2453-10dup
ENST00000406259.1:c.2624-15_2624-10dup	ENSP00000385444.1:n.2624-15_2624-10dup
ENST00000406522.5:c.2435-15_2435-10dup	ENSP00000384732.1:n.2435-15_2435-10dup
ENST00000495096.5:n.1564-15_1564-10dup
NM_001670.2:c.2642-15_2642-10dup	NP_001661.1:n.2642-15_2642-10dup
XM_005261242.1:c.2624-15_2624-10dup	XP_005261299.1:n.2624-15_2624-10dup
XM_005261243.3:c.2624-15_2624-10dup	XP_005261300.1:n.2624-15_2624-10dup
XM_005261244.3:c.2624-15_2624-10dup	XP_005261301.1:n.2624-15_2624-10dup
XM_006724243.1:c.2642-15_2642-10dup	XP_006724306.1:n.2642-15_2642-10dup
XM_006724245.2:c.2642-15_2642-10dup	XP_006724308.1:n.2642-15_2642-10dup
XM_006724246.2:c.2396-15_2396-10dup	XP_006724309.1:n.2396-15_2396-10dup
XM_006724247.2:c.2453-15_2453-10dup	XP_006724310.1:n.2453-15_2453-10dup
XM_006724248.2:c.2435-15_2435-10dup	XP_006724311.1:n.2435-15_2435-10dup
XM_011530179.1:c.2609-15_2609-10dup	XP_011528481.1:n.2609-15_2609-10dup
XM_011530180.1:c.2642-15_2642-10dup	XP_011528482.1:n.2642-15_2642-10dup
XM_011530182.1:c.1208-15_1208-10dup	XP_011528484.1:n.1208-15_1208-10dup
XM_011530183.1:c.1190-15_1190-10dup	XP_011528485.1:n.1190-15_1190-10dup
XR_937863.1:n.2729-15_2729-10dup
XR_937864.1:n.2729-15_2729-10dup
XM_005261242.3:c.2624-15_2624-10dup	XP_005261299.1:n.2624-15_2624-10dup
XM_005261243.4:c.2624-15_2624-10dup	XP_005261300.1:n.2624-15_2624-10dup
XM_005261244.4:c.2624-15_2624-10dup	XP_005261301.1:n.2624-15_2624-10dup
XM_006724243.3:c.2642-15_2642-10dup	XP_006724306.1:n.2642-15_2642-10dup
XM_006724245.3:c.2642-15_2642-10dup	XP_006724308.1:n.2642-15_2642-10dup
XM_006724246.4:c.2396-15_2396-10dup	XP_006724309.1:n.2396-15_2396-10dup
XM_006724247.4:c.2453-15_2453-10dup	XP_006724310.1:n.2453-15_2453-10dup
XM_006724248.4:c.2435-15_2435-10dup	XP_006724311.1:n.2435-15_2435-10dup
XM_011530179.3:c.2609-15_2609-10dup	XP_011528481.1:n.2609-15_2609-10dup
XM_011530182.3:c.1208-15_1208-10dup	XP_011528484.1:n.1208-15_1208-10dup
XM_011530183.3:c.1190-15_1190-10dup	XP_011528485.1:n.1190-15_1190-10dup
XM_024452249.1:c.2396-15_2396-10dup	XP_024308017.1:n.2396-15_2396-10dup
XR_937863.2:n.2729-15_2729-10dup
NM_001670.3:c.2642-15_2642-10dup MANE Select	NP_001661.1:n.2642-15_2642-10dup