Canonical Allele Identifier: CA1142376471
Gene: ARV1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.230988440G= , CM000663.2:g.230988440G= GRCh38
NC_000001.10:g.231124186G= , CM000663.1:g.231124186G= GRCh37
NC_000001.9:g.229190809G= NCBI36
NG_052022.1:g.14392G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000310256.7:c.294+1G= MANE Select ENSP00000312458.2:n.294+1G=
ENST00000310256.6:c.294+1G= ENSP00000312458.2:n.294+1G=
ENST00000366658.6:c.175-1670G= ENSP00000355618.2:n.175-1670G=
ENST00000435927.5:c.254+1G=
ENST00000450711.5:c.284+1G=
ENST00000480519.5:c.222+1G= ENSP00000436763.1:n.222+1G=
ENST00000497753.1:n.659+1G=
NM_022786.1:c.294+1G= NP_073623.1:n.294+1G=
XR_949154.1:n.325+1G=
NM_001346992.1:c.294+1G= NP_001333921.1:n.294+1G=
NM_022786.2:c.294+1G= NP_073623.1:n.294+1G=
NR_144538.1:n.351+1G=
XM_024449202.1:c.294+1G= XP_024304970.1:n.294+1G=
XR_002957381.1:n.318+1G=
NM_022786.3:c.294+1G= MANE Select NP_073623.1:n.294+1G=
NM_001346992.2:c.294+1G= NP_001333921.1:n.294+1G=
NR_144538.2:n.306+1G=