Canonical Allele Identifier: CA394913122
Community Standard Title: NM_015161.3(ARL6IP1):c.92T>C (p.Leu31Pro)
Gene: ARL6IP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.18798779A>G , CM000678.2:g.18798779A>G GRCh38
NC_000016.9:g.18810101A>G , CM000678.1:g.18810101A>G GRCh37
NC_000016.8:g.18717602A>G NCBI36
NG_042860.1:g.7900T>C

Transcript Alleles

HGVS Amino-acid Change
NM_015161.3:c.92T>C MANE Select NP_055976.1:p.Leu31Pro
ENST00000304414.12:c.92T>C MANE Select ENSP00000306788.7:p.Leu31Pro
NM_001313858.1:c.5T>C NP_001300787.1:p.Leu2Pro
NM_015161.1:c.92T>C NP_055976.1:p.Leu31Pro
NM_015161.2:c.92T>C NP_055976.1:p.Leu31Pro
ENST00000304414.11:c.92T>C ENSP00000306788.7:p.Leu31Pro
ENST00000546206.6:c.5T>C ENSP00000440048.2:p.Leu2Pro
ENST00000562234.2:c.92T>C ENSP00000455341.2:p.Leu31Pro
ENST00000562819.5:c.92T>C ENSP00000457372.1:p.Leu31Pro
ENST00000563861.5:c.92T>C ENSP00000456596.1:p.Leu31Pro
ENST00000566391.1:n.198T>C
ENST00000567078.2:c.92T>C ENSP00000454746.2:p.Leu31Pro
ENST00000567969.1:n.170T>C
ENST00000569976.5:n.174T>C