Canonical Allele Identifier: CA925522936
Gene: ARL5B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.18661626T>A , CM000672.2:g.18661626T>A GRCh38
NC_000010.10:g.18950555T>A , CM000672.1:g.18950555T>A GRCh37
NC_000010.9:g.18990561T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377275.4:c.46+1943T>A MANE Select ENSP00000366487.3:n.46+1943T>A
ENST00000377275.3:c.46+1943T>A ENSP00000366487.3:n.46+1943T>A
NM_178815.3:c.46+1943T>A NP_848930.1:n.46+1943T>A
XM_005252400.1:c.46+1943T>A XP_005252457.1:n.46+1943T>A
XM_005252401.3:c.-66+1734T>A XP_005252458.1:n.-66+1734T>A
NM_178815.4:c.46+1943T>A NP_848930.1:n.46+1943T>A
XM_005252401.4:c.-66+1734T>A XP_005252458.1:n.-66+1734T>A
NM_178815.5:c.46+1943T>A MANE Select NP_848930.1:n.46+1943T>A