Canonical Allele Identifier: CA2396130598

Gene: ARVCF

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19972451_19972452delinsCA , CM000684.2:g.19972451_19972452delinsCA	GRCh38
NC_000022.10:g.19959974_19959975delinsCA , CM000684.1:g.19959974_19959975delinsCA	GRCh37
NC_000022.9:g.18339974_18339975delinsCA	NCBI36
NG_023326.1:g.49335_49336delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263207.8:c.2642-41_2642-40delinsTG MANE Select	ENSP00000263207.3:n.2642-41_2642-40delinsTG
ENST00000263207.7:c.2642-41_2642-40delinsTG	ENSP00000263207.3:n.2642-41_2642-40delinsTG
ENST00000401994.5:c.2453-41_2453-40delinsTG	ENSP00000384341.1:n.2453-41_2453-40delinsTG
ENST00000406259.1:c.2624-41_2624-40delinsTG	ENSP00000385444.1:n.2624-41_2624-40delinsTG
ENST00000406522.5:c.2435-41_2435-40delinsTG	ENSP00000384732.1:n.2435-41_2435-40delinsTG
ENST00000495096.5:n.1564-41_1564-40delinsTG
NM_001670.2:c.2642-41_2642-40delinsTG	NP_001661.1:n.2642-41_2642-40delinsTG
XM_005261242.1:c.2624-41_2624-40delinsTG	XP_005261299.1:n.2624-41_2624-40delinsTG
XM_005261243.3:c.2624-41_2624-40delinsTG	XP_005261300.1:n.2624-41_2624-40delinsTG
XM_005261244.3:c.2624-41_2624-40delinsTG	XP_005261301.1:n.2624-41_2624-40delinsTG
XM_006724243.1:c.2642-41_2642-40delinsTG	XP_006724306.1:n.2642-41_2642-40delinsTG
XM_006724245.2:c.2642-41_2642-40delinsTG	XP_006724308.1:n.2642-41_2642-40delinsTG
XM_006724246.2:c.2396-41_2396-40delinsTG	XP_006724309.1:n.2396-41_2396-40delinsTG
XM_006724247.2:c.2453-41_2453-40delinsTG	XP_006724310.1:n.2453-41_2453-40delinsTG
XM_006724248.2:c.2435-41_2435-40delinsTG	XP_006724311.1:n.2435-41_2435-40delinsTG
XM_011530179.1:c.2609-41_2609-40delinsTG	XP_011528481.1:n.2609-41_2609-40delinsTG
XM_011530180.1:c.2642-41_2642-40delinsTG	XP_011528482.1:n.2642-41_2642-40delinsTG
XM_011530182.1:c.1208-41_1208-40delinsTG	XP_011528484.1:n.1208-41_1208-40delinsTG
XM_011530183.1:c.1190-41_1190-40delinsTG	XP_011528485.1:n.1190-41_1190-40delinsTG
XR_937863.1:n.2729-41_2729-40delinsTG
XR_937864.1:n.2729-41_2729-40delinsTG
XM_005261242.3:c.2624-41_2624-40delinsTG	XP_005261299.1:n.2624-41_2624-40delinsTG
XM_005261243.4:c.2624-41_2624-40delinsTG	XP_005261300.1:n.2624-41_2624-40delinsTG
XM_005261244.4:c.2624-41_2624-40delinsTG	XP_005261301.1:n.2624-41_2624-40delinsTG
XM_006724243.3:c.2642-41_2642-40delinsTG	XP_006724306.1:n.2642-41_2642-40delinsTG
XM_006724245.3:c.2642-41_2642-40delinsTG	XP_006724308.1:n.2642-41_2642-40delinsTG
XM_006724246.4:c.2396-41_2396-40delinsTG	XP_006724309.1:n.2396-41_2396-40delinsTG
XM_006724247.4:c.2453-41_2453-40delinsTG	XP_006724310.1:n.2453-41_2453-40delinsTG
XM_006724248.4:c.2435-41_2435-40delinsTG	XP_006724311.1:n.2435-41_2435-40delinsTG
XM_011530179.3:c.2609-41_2609-40delinsTG	XP_011528481.1:n.2609-41_2609-40delinsTG
XM_011530182.3:c.1208-41_1208-40delinsTG	XP_011528484.1:n.1208-41_1208-40delinsTG
XM_011530183.3:c.1190-41_1190-40delinsTG	XP_011528485.1:n.1190-41_1190-40delinsTG
XM_024452249.1:c.2396-41_2396-40delinsTG	XP_024308017.1:n.2396-41_2396-40delinsTG
XR_937863.2:n.2729-41_2729-40delinsTG
NM_001670.3:c.2642-41_2642-40delinsTG MANE Select	NP_001661.1:n.2642-41_2642-40delinsTG