Canonical Allele Identifier: CA2396132021

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19974854_19974855delinsCA , CM000684.2:g.19974854_19974855delinsCA	GRCh38
NC_000022.10:g.19962377_19962378delinsCA , CM000684.1:g.19962377_19962378delinsCA	GRCh37
NC_000022.9:g.18342377_18342378delinsCA	NCBI36
NG_023326.1:g.46932_46933delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.1961-616_1961-615delinsTG MANE Select	ENSP00000263207.3:n.1961-616_1961-615delinsTG
ENST00000263207.7:c.1961-616_1961-615delinsTG	ENSP00000263207.3:n.1961-616_1961-615delinsTG
ENST00000401994.5:c.1772-616_1772-615delinsTG	ENSP00000384341.1:n.1772-616_1772-615delinsTG
ENST00000406259.1:c.1943-616_1943-615delinsTG	ENSP00000385444.1:n.1943-616_1943-615delinsTG
ENST00000406522.5:c.1754-616_1754-615delinsTG	ENSP00000384732.1:n.1754-616_1754-615delinsTG
ENST00000480792.1:n.78-577_78-576delinsTG
ENST00000495096.5:n.883-616_883-615delinsTG
NM_001670.2:c.1961-616_1961-615delinsTG	NP_001661.1:n.1961-616_1961-615delinsTG
XM_005261242.1:c.1943-616_1943-615delinsTG	XP_005261299.1:n.1943-616_1943-615delinsTG
XM_005261243.3:c.1943-616_1943-615delinsTG	XP_005261300.1:n.1943-616_1943-615delinsTG
XM_005261244.3:c.1943-616_1943-615delinsTG	XP_005261301.1:n.1943-616_1943-615delinsTG
XM_006724243.1:c.1961-616_1961-615delinsTG	XP_006724306.1:n.1961-616_1961-615delinsTG
XM_006724245.2:c.1961-616_1961-615delinsTG	XP_006724308.1:n.1961-616_1961-615delinsTG
XM_006724246.2:c.1715-616_1715-615delinsTG	XP_006724309.1:n.1715-616_1715-615delinsTG
XM_006724247.2:c.1772-616_1772-615delinsTG	XP_006724310.1:n.1772-616_1772-615delinsTG
XM_006724248.2:c.1754-616_1754-615delinsTG	XP_006724311.1:n.1754-616_1754-615delinsTG
XM_006724249.2:c.1961-368_1961-367delinsTG	XP_006724312.1:n.1961-368_1961-367delinsTG
XM_006724250.2:c.1943-368_1943-367delinsTG	XP_006724313.1:n.1943-368_1943-367delinsTG
XM_011530179.1:c.1928-616_1928-615delinsTG	XP_011528481.1:n.1928-616_1928-615delinsTG
XM_011530180.1:c.1961-616_1961-615delinsTG	XP_011528482.1:n.1961-616_1961-615delinsTG
XM_011530182.1:c.527-616_527-615delinsTG	XP_011528484.1:n.527-616_527-615delinsTG
XM_011530183.1:c.509-616_509-615delinsTG	XP_011528485.1:n.509-616_509-615delinsTG
XR_937863.1:n.2247-616_2247-615delinsTG
XR_937864.1:n.2247-616_2247-615delinsTG
XM_005261242.3:c.1943-616_1943-615delinsTG	XP_005261299.1:n.1943-616_1943-615delinsTG
XM_005261243.4:c.1943-616_1943-615delinsTG	XP_005261300.1:n.1943-616_1943-615delinsTG
XM_005261244.4:c.1943-616_1943-615delinsTG	XP_005261301.1:n.1943-616_1943-615delinsTG
XM_006724243.3:c.1961-616_1961-615delinsTG	XP_006724306.1:n.1961-616_1961-615delinsTG
XM_006724245.3:c.1961-616_1961-615delinsTG	XP_006724308.1:n.1961-616_1961-615delinsTG
XM_006724246.4:c.1715-616_1715-615delinsTG	XP_006724309.1:n.1715-616_1715-615delinsTG
XM_006724247.4:c.1772-616_1772-615delinsTG	XP_006724310.1:n.1772-616_1772-615delinsTG
XM_006724248.4:c.1754-616_1754-615delinsTG	XP_006724311.1:n.1754-616_1754-615delinsTG
XM_006724249.3:c.1961-368_1961-367delinsTG	XP_006724312.1:n.1961-368_1961-367delinsTG
XM_006724250.3:c.1943-368_1943-367delinsTG	XP_006724313.1:n.1943-368_1943-367delinsTG
XM_011530179.3:c.1928-616_1928-615delinsTG	XP_011528481.1:n.1928-616_1928-615delinsTG
XM_011530182.3:c.527-616_527-615delinsTG	XP_011528484.1:n.527-616_527-615delinsTG
XM_011530183.3:c.509-616_509-615delinsTG	XP_011528485.1:n.509-616_509-615delinsTG
XM_024452249.1:c.1715-616_1715-615delinsTG	XP_024308017.1:n.1715-616_1715-615delinsTG
XR_937863.2:n.2247-616_2247-615delinsTG
NM_001670.3:c.1961-616_1961-615delinsTG MANE Select	NP_001661.1:n.1961-616_1961-615delinsTG