Canonical Allele Identifier: CA410694728

Gene: ARVCF

Linked Data

• MyVariant Identifiers: chr22:g.19960507T>C (hg19) ; chr22:g.19972984T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972984T>C , CM000684.2:g.19972984T>C	GRCh38
NC_000022.10:g.19960507T>C , CM000684.1:g.19960507T>C	GRCh37
NC_000022.9:g.18340507T>C	NCBI36
NG_023326.1:g.48803A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2491A>G MANE Select	ENSP00000263207.3:p.Ser831Gly
ENST00000263207.7:c.2491A>G	ENSP00000263207.3:p.Ser831Gly
ENST00000401994.5:c.2302A>G	ENSP00000384341.1:p.Ser768Gly
ENST00000406259.1:c.2473A>G	ENSP00000385444.1:p.Ser825Gly
ENST00000406522.5:c.2284A>G	ENSP00000384732.1:p.Ser762Gly
ENST00000495096.5:n.1413A>G
NM_001670.2:c.2491A>G	NP_001661.1:p.Ser831Gly
XM_005261242.1:c.2473A>G	XP_005261299.1:p.Ser825Gly
XM_005261243.3:c.2473A>G	XP_005261300.1:p.Ser825Gly
XM_005261244.3:c.2473A>G	XP_005261301.1:p.Ser825Gly
XM_006724243.1:c.2491A>G	XP_006724306.1:p.Ser831Gly
XM_006724245.2:c.2491A>G	XP_006724308.1:p.Ser831Gly
XM_006724246.2:c.2245A>G	XP_006724309.1:p.Ser749Gly
XM_006724247.2:c.2302A>G	XP_006724310.1:p.Ser768Gly
XM_006724248.2:c.2284A>G	XP_006724311.1:p.Ser762Gly
XM_011530179.1:c.2458A>G	XP_011528481.1:p.Ser820Gly
XM_011530180.1:c.2491A>G	XP_011528482.1:p.Ser831Gly
XM_011530182.1:c.1057A>G	XP_011528484.1:p.Ser353Gly
XM_011530183.1:c.1039A>G	XP_011528485.1:p.Ser347Gly
XR_937863.1:n.2578A>G
XR_937864.1:n.2578A>G
XM_005261242.3:c.2473A>G	XP_005261299.1:p.Ser825Gly
XM_005261243.4:c.2473A>G	XP_005261300.1:p.Ser825Gly
XM_005261244.4:c.2473A>G	XP_005261301.1:p.Ser825Gly
XM_006724243.3:c.2491A>G	XP_006724306.1:p.Ser831Gly
XM_006724245.3:c.2491A>G	XP_006724308.1:p.Ser831Gly
XM_006724246.4:c.2245A>G	XP_006724309.1:p.Ser749Gly
XM_006724247.4:c.2302A>G	XP_006724310.1:p.Ser768Gly
XM_006724248.4:c.2284A>G	XP_006724311.1:p.Ser762Gly
XM_011530179.3:c.2458A>G	XP_011528481.1:p.Ser820Gly
XM_011530182.3:c.1057A>G	XP_011528484.1:p.Ser353Gly
XM_011530183.3:c.1039A>G	XP_011528485.1:p.Ser347Gly
XM_024452249.1:c.2245A>G	XP_024308017.1:p.Ser749Gly
XR_937863.2:n.2578A>G
NM_001670.3:c.2491A>G MANE Select	NP_001661.1:p.Ser831Gly