Canonical Allele Identifier: CA2546683789

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19996779A>C , CM000684.2:g.19996779A>C	GRCh38
NC_000022.10:g.19984302A>C , CM000684.1:g.19984302A>C	GRCh37
NC_000022.9:g.18364302A>C	NCBI36
NG_023326.1:g.25008T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000263207.8:c.-18-5967T>G MANE Select	ENSP00000263207.3:n.-18-5967T>G
ENST00000263207.7:c.-18-5967T>G	ENSP00000263207.3:n.-18-5967T>G
ENST00000467828.1:n.158-14688T>G
NM_001670.2:c.-18-5967T>G	NP_001661.1:n.-18-5967T>G
XM_005261242.1:c.-18-5967T>G	XP_005261299.1:n.-18-5967T>G
XM_005261243.3:c.-18-5967T>G	XP_005261300.1:n.-18-5967T>G
XM_005261244.3:c.-18-5967T>G	XP_005261301.1:n.-18-5967T>G
XM_006724243.1:c.-18-5967T>G	XP_006724306.1:n.-18-5967T>G
XM_006724245.2:c.-18-5967T>G	XP_006724308.1:n.-18-5967T>G
XM_006724249.2:c.-18-5967T>G	XP_006724312.1:n.-18-5967T>G
XM_006724250.2:c.-18-5967T>G	XP_006724313.1:n.-18-5967T>G
XM_011530179.1:c.-18-5967T>G	XP_011528481.1:n.-18-5967T>G
XM_011530180.1:c.-18-5967T>G	XP_011528482.1:n.-18-5967T>G
XM_011530181.1:c.-18-5967T>G	XP_011528483.1:n.-18-5967T>G
XR_937863.1:n.269-5967T>G
XR_937864.1:n.269-5967T>G
XM_005261242.3:c.-18-5967T>G	XP_005261299.1:n.-18-5967T>G
XM_005261243.4:c.-18-5967T>G	XP_005261300.1:n.-18-5967T>G
XM_005261244.4:c.-18-5967T>G	XP_005261301.1:n.-18-5967T>G
XM_006724243.3:c.-18-5967T>G	XP_006724306.1:n.-18-5967T>G
XM_006724245.3:c.-18-5967T>G	XP_006724308.1:n.-18-5967T>G
XM_006724249.3:c.-18-5967T>G	XP_006724312.1:n.-18-5967T>G
XM_006724250.3:c.-18-5967T>G	XP_006724313.1:n.-18-5967T>G
XM_011530179.3:c.-18-5967T>G	XP_011528481.1:n.-18-5967T>G
XR_937863.2:n.269-5967T>G
NM_001670.3:c.-18-5967T>G MANE Select	NP_001661.1:n.-18-5967T>G