Canonical Allele Identifier: CA374158625
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343416C>G , CM000671.2:g.97343416C>G GRCh38
NC_000009.11:g.100105698C>G , CM000671.1:g.100105698C>G GRCh37
NC_000009.10:g.99145519C>G NCBI36
NG_052792.1:g.41113C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529487.3:c.2351C>G (CCDC180) MANE Select ENSP00000434727.2:p.Thr784Ser
ENST00000460482.6:n.2685C>G (CCDC180)
ENST00000494917.6:n.2554C>G (CCDC180)
ENST00000528678.1:n.447C>G (CCDC180)
ENST00000529487.1:c.2483C>G (CCDC180) ENSP00000434727.1:p.Thr828Ser
ENST00000530011.1:n.236-5695C>G (CCDC180)
NM_020893.2:c.2483C>G (CCDC180) NP_065944.2:p.Thr828Ser
NR_036527.1:n.3906C>G (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3906C>G (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3466C>G (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2474C>G (CCDC180) NP_001334939.1:p.Thr825Ser
NM_020893.3:c.2483C>G (CCDC180) NP_065944.2:p.Thr828Ser
NM_001348010.2:c.2474C>G (CCDC180) NP_001334939.1:p.Thr825Ser
NM_020893.4:c.2483C>G (CCDC180) NP_065944.2:p.Thr828Ser
NM_001348010.4:c.2342C>G (CCDC180) NP_001334939.2:p.Thr781Ser
NM_020893.6:c.2351C>G (CCDC180) MANE Select NP_065944.3:p.Thr784Ser