Canonical Allele Identifier: CA2396130942

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972998A= , CM000684.2:g.19972998A=	GRCh38
NC_000022.10:g.19960521A= , CM000684.1:g.19960521A=	GRCh37
NC_000022.9:g.18340521A=	NCBI36
NG_023326.1:g.48789T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2477T= MANE Select	ENSP00000263207.3:p.Leu826=
ENST00000263207.7:c.2477T=	ENSP00000263207.3:p.Leu826=
ENST00000401994.5:c.2288T=	ENSP00000384341.1:p.Leu763=
ENST00000406259.1:c.2459T=	ENSP00000385444.1:p.Leu820=
ENST00000406522.5:c.2270T=	ENSP00000384732.1:p.Leu757=
ENST00000495096.5:n.1399T=
NM_001670.2:c.2477T=	NP_001661.1:p.Leu826=
XM_005261242.1:c.2459T=	XP_005261299.1:p.Leu820=
XM_005261243.3:c.2459T=	XP_005261300.1:p.Leu820=
XM_005261244.3:c.2459T=	XP_005261301.1:p.Leu820=
XM_006724243.1:c.2477T=	XP_006724306.1:p.Leu826=
XM_006724245.2:c.2477T=	XP_006724308.1:p.Leu826=
XM_006724246.2:c.2231T=	XP_006724309.1:p.Leu744=
XM_006724247.2:c.2288T=	XP_006724310.1:p.Leu763=
XM_006724248.2:c.2270T=	XP_006724311.1:p.Leu757=
XM_011530179.1:c.2444T=	XP_011528481.1:p.Leu815=
XM_011530180.1:c.2477T=	XP_011528482.1:p.Leu826=
XM_011530182.1:c.1043T=	XP_011528484.1:p.Leu348=
XM_011530183.1:c.1025T=	XP_011528485.1:p.Leu342=
XR_937863.1:n.2564T=
XR_937864.1:n.2564T=
XM_005261242.3:c.2459T=	XP_005261299.1:p.Leu820=
XM_005261243.4:c.2459T=	XP_005261300.1:p.Leu820=
XM_005261244.4:c.2459T=	XP_005261301.1:p.Leu820=
XM_006724243.3:c.2477T=	XP_006724306.1:p.Leu826=
XM_006724245.3:c.2477T=	XP_006724308.1:p.Leu826=
XM_006724246.4:c.2231T=	XP_006724309.1:p.Leu744=
XM_006724247.4:c.2288T=	XP_006724310.1:p.Leu763=
XM_006724248.4:c.2270T=	XP_006724311.1:p.Leu757=
XM_011530179.3:c.2444T=	XP_011528481.1:p.Leu815=
XM_011530182.3:c.1043T=	XP_011528484.1:p.Leu348=
XM_011530183.3:c.1025T=	XP_011528485.1:p.Leu342=
XM_024452249.1:c.2231T=	XP_024308017.1:p.Leu744=
XR_937863.2:n.2564T=
NM_001670.3:c.2477T= MANE Select	NP_001661.1:p.Leu826=