Canonical Allele Identifier: CA2838480564
Gene: ARRDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.137612864G>T , CM000671.2:g.137612864G>T GRCh38
NC_000009.11:g.140507316G>T , CM000671.1:g.140507316G>T GRCh37
NC_000009.10:g.139627137G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000371421.9:c.119-32G>T MANE Select ENSP00000360475.4:n.119-32G>T
ENST00000371421.8:c.119-32G>T ENSP00000360475.4:n.119-32G>T
ENST00000419386.1:c.119-32G>T ENSP00000406833.1:n.119-32G>T
ENST00000431925.6:c.119-32G>T ENSP00000406247.2:n.119-32G>T
ENST00000461627.1:c.119-32G>T ENSP00000435996.1:n.119-32G>T
ENST00000466367.5:n.108-32G>T
ENST00000471125.5:n.96-32G>T
ENST00000483563.5:n.152-32G>T
ENST00000491911.5:n.1414G>T
ENST00000495220.5:n.96-32G>T
ENST00000497877.5:n.123-32G>T
NM_152285.2:c.119-32G>T NP_689498.1:n.119-32G>T
XM_005266119.1:c.119-32G>T XP_005266176.1:n.119-32G>T
XM_005266121.1:c.119-32G>T XP_005266178.1:n.119-32G>T
XM_006717320.2:c.108G>T XP_006717383.1:p.Leu36=
XM_006717321.2:c.108G>T XP_006717384.1:p.Leu36=
XM_006717322.2:c.108G>T XP_006717385.1:p.Leu36=
NM_001317968.1:c.119-32G>T NP_001304897.1:n.119-32G>T
NM_152285.3:c.119-32G>T NP_689498.1:n.119-32G>T
XM_006717320.4:c.108G>T XP_006717383.1:p.Leu36=
XM_006717321.4:c.108G>T XP_006717384.1:p.Leu36=
XM_006717322.4:c.108G>T XP_006717385.1:p.Leu36=
XM_017015288.2:c.108G>T XP_016870777.1:p.Leu36=
XM_024447713.1:c.-972-32G>T XP_024303481.1:n.-972-32G>T
XM_024447714.1:c.-566-32G>T XP_024303482.1:n.-566-32G>T
NM_152285.4:c.119-32G>T MANE Select NP_689498.1:n.119-32G>T
NM_001317968.2:c.119-32G>T NP_001304897.1:n.119-32G>T