Canonical Allele Identifier: CA466159162
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.100105789C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343507C>A , CM000671.2:g.97343507C>A GRCh38
NC_000009.11:g.100105789C>A , CM000671.1:g.100105789C>A GRCh37
NC_000009.10:g.99145610C>A NCBI36
NG_052792.1:g.41204C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000529487.3:c.2442C>A (CCDC180) MANE Select ENSP00000434727.2:p.Ala814=
ENST00000460482.6:n.2776C>A (CCDC180)
ENST00000494917.6:n.2645C>A (CCDC180)
ENST00000528678.1:n.538C>A (CCDC180)
ENST00000529487.1:c.2574C>A (CCDC180) ENSP00000434727.1:p.Ala858=
ENST00000530011.1:n.236-5604C>A (CCDC180)
NM_020893.2:c.2574C>A (CCDC180) NP_065944.2:p.Ala858=
NR_036527.1:n.3997C>A (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3997C>A (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3557C>A (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2565C>A (CCDC180) NP_001334939.1:p.Ala855=
NM_020893.3:c.2574C>A (CCDC180) NP_065944.2:p.Ala858=
NM_001348010.2:c.2565C>A (CCDC180) NP_001334939.1:p.Ala855=
NM_020893.4:c.2574C>A (CCDC180) NP_065944.2:p.Ala858=
NM_001348010.4:c.2433C>A (CCDC180) NP_001334939.2:p.Ala811=
NM_020893.6:c.2442C>A (CCDC180) MANE Select NP_065944.3:p.Ala814=