Canonical Allele Identifier: CA410693358

Gene: ARVCF

Linked Data

• MyVariant Identifiers: chr22:g.19959895T>C (hg19) ; chr22:g.19972372T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972372T>C , CM000684.2:g.19972372T>C	GRCh38
NC_000022.10:g.19959895T>C , CM000684.1:g.19959895T>C	GRCh37
NC_000022.9:g.18339895T>C	NCBI36
NG_023326.1:g.49415A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2681A>G MANE Select	ENSP00000263207.3:p.Asp894Gly
ENST00000263207.7:c.2681A>G	ENSP00000263207.3:p.Asp894Gly
ENST00000401994.5:c.2492A>G	ENSP00000384341.1:p.Asp831Gly
ENST00000406259.1:c.2663A>G	ENSP00000385444.1:p.Asp888Gly
ENST00000406522.5:c.2474A>G	ENSP00000384732.1:p.Asp825Gly
ENST00000495096.5:n.1603A>G
NM_001670.2:c.2681A>G	NP_001661.1:p.Asp894Gly
XM_005261242.1:c.2663A>G	XP_005261299.1:p.Asp888Gly
XM_005261243.3:c.2663A>G	XP_005261300.1:p.Asp888Gly
XM_005261244.3:c.2663A>G	XP_005261301.1:p.Asp888Gly
XM_006724243.1:c.2681A>G	XP_006724306.1:p.Asp894Gly
XM_006724245.2:c.2681A>G	XP_006724308.1:p.Asp894Gly
XM_006724246.2:c.2435A>G	XP_006724309.1:p.Asp812Gly
XM_006724247.2:c.2492A>G	XP_006724310.1:p.Asp831Gly
XM_006724248.2:c.2474A>G	XP_006724311.1:p.Asp825Gly
XM_011530179.1:c.2648A>G	XP_011528481.1:p.Asp883Gly
XM_011530180.1:c.2681A>G	XP_011528482.1:p.Asp894Gly
XM_011530182.1:c.1247A>G	XP_011528484.1:p.Asp416Gly
XM_011530183.1:c.1229A>G	XP_011528485.1:p.Asp410Gly
XR_937863.1:n.2768A>G
XR_937864.1:n.2768A>G
XM_005261242.3:c.2663A>G	XP_005261299.1:p.Asp888Gly
XM_005261243.4:c.2663A>G	XP_005261300.1:p.Asp888Gly
XM_005261244.4:c.2663A>G	XP_005261301.1:p.Asp888Gly
XM_006724243.3:c.2681A>G	XP_006724306.1:p.Asp894Gly
XM_006724245.3:c.2681A>G	XP_006724308.1:p.Asp894Gly
XM_006724246.4:c.2435A>G	XP_006724309.1:p.Asp812Gly
XM_006724247.4:c.2492A>G	XP_006724310.1:p.Asp831Gly
XM_006724248.4:c.2474A>G	XP_006724311.1:p.Asp825Gly
XM_011530179.3:c.2648A>G	XP_011528481.1:p.Asp883Gly
XM_011530182.3:c.1247A>G	XP_011528484.1:p.Asp416Gly
XM_011530183.3:c.1229A>G	XP_011528485.1:p.Asp410Gly
XM_024452249.1:c.2435A>G	XP_024308017.1:p.Asp812Gly
XR_937863.2:n.2768A>G
NM_001670.3:c.2681A>G MANE Select	NP_001661.1:p.Asp894Gly