Canonical Allele Identifier: CA513365576

Gene: ARVCF

Linked Data

• dbSNP Id: rs1942861191
• MyVariant Identifiers: chr22:g.19959888C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972365C>T , CM000684.2:g.19972365C>T	GRCh38
NC_000022.10:g.19959888C>T , CM000684.1:g.19959888C>T	GRCh37
NC_000022.9:g.18339888C>T	NCBI36
NG_023326.1:g.49422G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2688G>A MANE Select	ENSP00000263207.3:p.Leu896=
ENST00000263207.7:c.2688G>A	ENSP00000263207.3:p.Leu896=
ENST00000401994.5:c.2499G>A	ENSP00000384341.1:p.Leu833=
ENST00000406259.1:c.2670G>A	ENSP00000385444.1:p.Leu890=
ENST00000406522.5:c.2481G>A	ENSP00000384732.1:p.Leu827=
ENST00000495096.5:n.1610G>A
NM_001670.2:c.2688G>A	NP_001661.1:p.Leu896=
XM_005261242.1:c.2670G>A	XP_005261299.1:p.Leu890=
XM_005261243.3:c.2670G>A	XP_005261300.1:p.Leu890=
XM_005261244.3:c.2670G>A	XP_005261301.1:p.Leu890=
XM_006724243.1:c.2688G>A	XP_006724306.1:p.Leu896=
XM_006724245.2:c.2688G>A	XP_006724308.1:p.Leu896=
XM_006724246.2:c.2442G>A	XP_006724309.1:p.Leu814=
XM_006724247.2:c.2499G>A	XP_006724310.1:p.Leu833=
XM_006724248.2:c.2481G>A	XP_006724311.1:p.Leu827=
XM_011530179.1:c.2655G>A	XP_011528481.1:p.Leu885=
XM_011530180.1:c.2688G>A	XP_011528482.1:p.Leu896=
XM_011530182.1:c.1254G>A	XP_011528484.1:p.Leu418=
XM_011530183.1:c.1236G>A	XP_011528485.1:p.Leu412=
XR_937863.1:n.2775G>A
XR_937864.1:n.2775G>A
XM_005261242.3:c.2670G>A	XP_005261299.1:p.Leu890=
XM_005261243.4:c.2670G>A	XP_005261300.1:p.Leu890=
XM_005261244.4:c.2670G>A	XP_005261301.1:p.Leu890=
XM_006724243.3:c.2688G>A	XP_006724306.1:p.Leu896=
XM_006724245.3:c.2688G>A	XP_006724308.1:p.Leu896=
XM_006724246.4:c.2442G>A	XP_006724309.1:p.Leu814=
XM_006724247.4:c.2499G>A	XP_006724310.1:p.Leu833=
XM_006724248.4:c.2481G>A	XP_006724311.1:p.Leu827=
XM_011530179.3:c.2655G>A	XP_011528481.1:p.Leu885=
XM_011530182.3:c.1254G>A	XP_011528484.1:p.Leu418=
XM_011530183.3:c.1236G>A	XP_011528485.1:p.Leu412=
XM_024452249.1:c.2442G>A	XP_024308017.1:p.Leu814=
XR_937863.2:n.2775G>A
NM_001670.3:c.2688G>A MANE Select	NP_001661.1:p.Leu896=