Canonical Allele Identifier: CA2396130799

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972793G= , CM000684.2:g.19972793G=	GRCh38
NC_000022.10:g.19960316G= , CM000684.1:g.19960316G=	GRCh37
NC_000022.9:g.18340316G=	NCBI36
NG_023326.1:g.48994C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2585C= MANE Select	ENSP00000263207.3:p.Ala862=
ENST00000263207.7:c.2585C=	ENSP00000263207.3:p.Ala862=
ENST00000401994.5:c.2396C=	ENSP00000384341.1:p.Ala799=
ENST00000406259.1:c.2567C=	ENSP00000385444.1:p.Ala856=
ENST00000406522.5:c.2378C=	ENSP00000384732.1:p.Ala793=
ENST00000495096.5:n.1507C=
NM_001670.2:c.2585C=	NP_001661.1:p.Ala862=
XM_005261242.1:c.2567C=	XP_005261299.1:p.Ala856=
XM_005261243.3:c.2567C=	XP_005261300.1:p.Ala856=
XM_005261244.3:c.2567C=	XP_005261301.1:p.Ala856=
XM_006724243.1:c.2585C=	XP_006724306.1:p.Ala862=
XM_006724245.2:c.2585C=	XP_006724308.1:p.Ala862=
XM_006724246.2:c.2339C=	XP_006724309.1:p.Ala780=
XM_006724247.2:c.2396C=	XP_006724310.1:p.Ala799=
XM_006724248.2:c.2378C=	XP_006724311.1:p.Ala793=
XM_011530179.1:c.2552C=	XP_011528481.1:p.Ala851=
XM_011530180.1:c.2585C=	XP_011528482.1:p.Ala862=
XM_011530182.1:c.1151C=	XP_011528484.1:p.Ala384=
XM_011530183.1:c.1133C=	XP_011528485.1:p.Ala378=
XR_937863.1:n.2672C=
XR_937864.1:n.2672C=
XM_005261242.3:c.2567C=	XP_005261299.1:p.Ala856=
XM_005261243.4:c.2567C=	XP_005261300.1:p.Ala856=
XM_005261244.4:c.2567C=	XP_005261301.1:p.Ala856=
XM_006724243.3:c.2585C=	XP_006724306.1:p.Ala862=
XM_006724245.3:c.2585C=	XP_006724308.1:p.Ala862=
XM_006724246.4:c.2339C=	XP_006724309.1:p.Ala780=
XM_006724247.4:c.2396C=	XP_006724310.1:p.Ala799=
XM_006724248.4:c.2378C=	XP_006724311.1:p.Ala793=
XM_011530179.3:c.2552C=	XP_011528481.1:p.Ala851=
XM_011530182.3:c.1151C=	XP_011528484.1:p.Ala384=
XM_011530183.3:c.1133C=	XP_011528485.1:p.Ala378=
XM_024452249.1:c.2339C=	XP_024308017.1:p.Ala780=
XR_937863.2:n.2672C=
NM_001670.3:c.2585C= MANE Select	NP_001661.1:p.Ala862=