Canonical Allele Identifier: CA2818402550

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972697_19972698insT , CM000684.2:g.19972697_19972698insT	GRCh38
NC_000022.10:g.19960220_19960221insT , CM000684.1:g.19960220_19960221insT	GRCh37
NC_000022.9:g.18340220_18340221insT	NCBI36
NG_023326.1:g.49089_49090insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2641+39_2641+40insA MANE Select	ENSP00000263207.3:n.2641+39_2641+40insA
ENST00000263207.7:c.2641+39_2641+40insA	ENSP00000263207.3:n.2641+39_2641+40insA
ENST00000401994.5:c.2452+39_2452+40insA	ENSP00000384341.1:n.2452+39_2452+40insA
ENST00000406259.1:c.2623+39_2623+40insA	ENSP00000385444.1:n.2623+39_2623+40insA
ENST00000406522.5:c.2434+39_2434+40insA	ENSP00000384732.1:n.2434+39_2434+40insA
ENST00000495096.5:n.1563+39_1563+40insA
NM_001670.2:c.2641+39_2641+40insA	NP_001661.1:n.2641+39_2641+40insA
XM_005261242.1:c.2623+39_2623+40insA	XP_005261299.1:n.2623+39_2623+40insA
XM_005261243.3:c.2623+39_2623+40insA	XP_005261300.1:n.2623+39_2623+40insA
XM_005261244.3:c.2623+39_2623+40insA	XP_005261301.1:n.2623+39_2623+40insA
XM_006724243.1:c.2641+39_2641+40insA	XP_006724306.1:n.2641+39_2641+40insA
XM_006724245.2:c.2641+39_2641+40insA	XP_006724308.1:n.2641+39_2641+40insA
XM_006724246.2:c.2395+39_2395+40insA	XP_006724309.1:n.2395+39_2395+40insA
XM_006724247.2:c.2452+39_2452+40insA	XP_006724310.1:n.2452+39_2452+40insA
XM_006724248.2:c.2434+39_2434+40insA	XP_006724311.1:n.2434+39_2434+40insA
XM_011530179.1:c.2608+39_2608+40insA	XP_011528481.1:n.2608+39_2608+40insA
XM_011530180.1:c.2641+39_2641+40insA	XP_011528482.1:n.2641+39_2641+40insA
XM_011530182.1:c.1207+39_1207+40insA	XP_011528484.1:n.1207+39_1207+40insA
XM_011530183.1:c.1189+39_1189+40insA	XP_011528485.1:n.1189+39_1189+40insA
XR_937863.1:n.2728+39_2728+40insA
XR_937864.1:n.2728+39_2728+40insA
XM_005261242.3:c.2623+39_2623+40insA	XP_005261299.1:n.2623+39_2623+40insA
XM_005261243.4:c.2623+39_2623+40insA	XP_005261300.1:n.2623+39_2623+40insA
XM_005261244.4:c.2623+39_2623+40insA	XP_005261301.1:n.2623+39_2623+40insA
XM_006724243.3:c.2641+39_2641+40insA	XP_006724306.1:n.2641+39_2641+40insA
XM_006724245.3:c.2641+39_2641+40insA	XP_006724308.1:n.2641+39_2641+40insA
XM_006724246.4:c.2395+39_2395+40insA	XP_006724309.1:n.2395+39_2395+40insA
XM_006724247.4:c.2452+39_2452+40insA	XP_006724310.1:n.2452+39_2452+40insA
XM_006724248.4:c.2434+39_2434+40insA	XP_006724311.1:n.2434+39_2434+40insA
XM_011530179.3:c.2608+39_2608+40insA	XP_011528481.1:n.2608+39_2608+40insA
XM_011530182.3:c.1207+39_1207+40insA	XP_011528484.1:n.1207+39_1207+40insA
XM_011530183.3:c.1189+39_1189+40insA	XP_011528485.1:n.1189+39_1189+40insA
XM_024452249.1:c.2395+39_2395+40insA	XP_024308017.1:n.2395+39_2395+40insA
XR_937863.2:n.2728+39_2728+40insA
NM_001670.3:c.2641+39_2641+40insA MANE Select	NP_001661.1:n.2641+39_2641+40insA