Canonical Allele Identifier: CA394913080
Community Standard Title: NM_015161.3(ARL6IP1):c.112C>T (p.Arg38Ter)
Gene: ARL6IP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.18798759G>A , CM000678.2:g.18798759G>A GRCh38
NC_000016.9:g.18810081G>A , CM000678.1:g.18810081G>A GRCh37
NC_000016.8:g.18717582G>A NCBI36
NG_042860.1:g.7920C>T

Transcript Alleles

HGVS Amino-acid Change
NM_015161.3:c.112C>T MANE Select NP_055976.1:p.Arg38Ter
ENST00000304414.12:c.112C>T MANE Select ENSP00000306788.7:p.Arg38Ter
NM_001313858.1:c.25C>T NP_001300787.1:p.Arg9Ter
NM_015161.1:c.112C>T NP_055976.1:p.Arg38Ter
NM_015161.2:c.112C>T NP_055976.1:p.Arg38Ter
ENST00000304414.11:c.112C>T ENSP00000306788.7:p.Arg38Ter
ENST00000546206.6:c.25C>T ENSP00000440048.2:p.Arg9Ter
ENST00000562234.2:c.112C>T ENSP00000455341.2:p.Arg38Ter
ENST00000562819.5:c.112C>T ENSP00000457372.1:p.Arg38Ter
ENST00000563861.5:c.112C>T ENSP00000456596.1:p.Arg38Ter
ENST00000566391.1:n.218C>T
ENST00000567078.2:c.112C>T ENSP00000454746.2:p.Arg38Ter
ENST00000567969.1:n.190C>T
ENST00000569976.5:n.194C>T