Canonical Allele Identifier: CA2396130580

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972424A= , CM000684.2:g.19972424A=	GRCh38
NC_000022.10:g.19959947A= , CM000684.1:g.19959947A=	GRCh37
NC_000022.9:g.18339947A=	NCBI36
NG_023326.1:g.49363T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2642-13T= MANE Select	ENSP00000263207.3:n.2642-13T=
ENST00000263207.7:c.2642-13T=	ENSP00000263207.3:n.2642-13T=
ENST00000401994.5:c.2453-13T=	ENSP00000384341.1:n.2453-13T=
ENST00000406259.1:c.2624-13T=	ENSP00000385444.1:n.2624-13T=
ENST00000406522.5:c.2435-13T=	ENSP00000384732.1:n.2435-13T=
ENST00000495096.5:n.1564-13T=
NM_001670.2:c.2642-13T=	NP_001661.1:n.2642-13T=
XM_005261242.1:c.2624-13T=	XP_005261299.1:n.2624-13T=
XM_005261243.3:c.2624-13T=	XP_005261300.1:n.2624-13T=
XM_005261244.3:c.2624-13T=	XP_005261301.1:n.2624-13T=
XM_006724243.1:c.2642-13T=	XP_006724306.1:n.2642-13T=
XM_006724245.2:c.2642-13T=	XP_006724308.1:n.2642-13T=
XM_006724246.2:c.2396-13T=	XP_006724309.1:n.2396-13T=
XM_006724247.2:c.2453-13T=	XP_006724310.1:n.2453-13T=
XM_006724248.2:c.2435-13T=	XP_006724311.1:n.2435-13T=
XM_011530179.1:c.2609-13T=	XP_011528481.1:n.2609-13T=
XM_011530180.1:c.2642-13T=	XP_011528482.1:n.2642-13T=
XM_011530182.1:c.1208-13T=	XP_011528484.1:n.1208-13T=
XM_011530183.1:c.1190-13T=	XP_011528485.1:n.1190-13T=
XR_937863.1:n.2729-13T=
XR_937864.1:n.2729-13T=
XM_005261242.3:c.2624-13T=	XP_005261299.1:n.2624-13T=
XM_005261243.4:c.2624-13T=	XP_005261300.1:n.2624-13T=
XM_005261244.4:c.2624-13T=	XP_005261301.1:n.2624-13T=
XM_006724243.3:c.2642-13T=	XP_006724306.1:n.2642-13T=
XM_006724245.3:c.2642-13T=	XP_006724308.1:n.2642-13T=
XM_006724246.4:c.2396-13T=	XP_006724309.1:n.2396-13T=
XM_006724247.4:c.2453-13T=	XP_006724310.1:n.2453-13T=
XM_006724248.4:c.2435-13T=	XP_006724311.1:n.2435-13T=
XM_011530179.3:c.2609-13T=	XP_011528481.1:n.2609-13T=
XM_011530182.3:c.1208-13T=	XP_011528484.1:n.1208-13T=
XM_011530183.3:c.1190-13T=	XP_011528485.1:n.1190-13T=
XM_024452249.1:c.2396-13T=	XP_024308017.1:n.2396-13T=
XR_937863.2:n.2729-13T=
NM_001670.3:c.2642-13T= MANE Select	NP_001661.1:n.2642-13T=