Canonical Allele Identifier: CA410694854

Gene: ARVCF

Linked Data

• MyVariant Identifiers: chr22:g.19960537C>A (hg19) ; chr22:g.19973014C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19973014C>A , CM000684.2:g.19973014C>A	GRCh38
NC_000022.10:g.19960537C>A , CM000684.1:g.19960537C>A	GRCh37
NC_000022.9:g.18340537C>A	NCBI36
NG_023326.1:g.48773G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2461G>T MANE Select	ENSP00000263207.3:p.Ala821Ser
ENST00000263207.7:c.2461G>T	ENSP00000263207.3:p.Ala821Ser
ENST00000401994.5:c.2272G>T	ENSP00000384341.1:p.Ala758Ser
ENST00000406259.1:c.2443G>T	ENSP00000385444.1:p.Ala815Ser
ENST00000406522.5:c.2254G>T	ENSP00000384732.1:p.Ala752Ser
ENST00000495096.5:n.1383G>T
NM_001670.2:c.2461G>T	NP_001661.1:p.Ala821Ser
XM_005261242.1:c.2443G>T	XP_005261299.1:p.Ala815Ser
XM_005261243.3:c.2443G>T	XP_005261300.1:p.Ala815Ser
XM_005261244.3:c.2443G>T	XP_005261301.1:p.Ala815Ser
XM_006724243.1:c.2461G>T	XP_006724306.1:p.Ala821Ser
XM_006724245.2:c.2461G>T	XP_006724308.1:p.Ala821Ser
XM_006724246.2:c.2215G>T	XP_006724309.1:p.Ala739Ser
XM_006724247.2:c.2272G>T	XP_006724310.1:p.Ala758Ser
XM_006724248.2:c.2254G>T	XP_006724311.1:p.Ala752Ser
XM_011530179.1:c.2428G>T	XP_011528481.1:p.Ala810Ser
XM_011530180.1:c.2461G>T	XP_011528482.1:p.Ala821Ser
XM_011530182.1:c.1027G>T	XP_011528484.1:p.Ala343Ser
XM_011530183.1:c.1009G>T	XP_011528485.1:p.Ala337Ser
XR_937863.1:n.2548G>T
XR_937864.1:n.2548G>T
XM_005261242.3:c.2443G>T	XP_005261299.1:p.Ala815Ser
XM_005261243.4:c.2443G>T	XP_005261300.1:p.Ala815Ser
XM_005261244.4:c.2443G>T	XP_005261301.1:p.Ala815Ser
XM_006724243.3:c.2461G>T	XP_006724306.1:p.Ala821Ser
XM_006724245.3:c.2461G>T	XP_006724308.1:p.Ala821Ser
XM_006724246.4:c.2215G>T	XP_006724309.1:p.Ala739Ser
XM_006724247.4:c.2272G>T	XP_006724310.1:p.Ala758Ser
XM_006724248.4:c.2254G>T	XP_006724311.1:p.Ala752Ser
XM_011530179.3:c.2428G>T	XP_011528481.1:p.Ala810Ser
XM_011530182.3:c.1027G>T	XP_011528484.1:p.Ala343Ser
XM_011530183.3:c.1009G>T	XP_011528485.1:p.Ala337Ser
XM_024452249.1:c.2215G>T	XP_024308017.1:p.Ala739Ser
XR_937863.2:n.2548G>T
NM_001670.3:c.2461G>T MANE Select	NP_001661.1:p.Ala821Ser