Canonical Allele Identifier: CA5145553
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

dbSNP Id: rs538222186
gnomAD v3: 9-97343375-C-T
gnomAD v4: 9-97343375-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343375C>T , CM000671.2:g.97343375C>T GRCh38
NC_000009.11:g.100105657C>T , CM000671.1:g.100105657C>T GRCh37
NC_000009.10:g.99145478C>T NCBI36
NG_052792.1:g.41072C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529487.3:c.2310C>T (CCDC180) MANE Select ENSP00000434727.2:p.Tyr770=
ENST00000460482.6:n.2644C>T (CCDC180)
ENST00000494917.6:n.2513C>T (CCDC180)
ENST00000528678.1:n.406C>T (CCDC180)
ENST00000529487.1:c.2442C>T (CCDC180) ENSP00000434727.1:p.Tyr814=
ENST00000530011.1:n.236-5736C>T (CCDC180)
NM_020893.2:c.2442C>T (CCDC180) NP_065944.2:p.Tyr814=
NR_036527.1:n.3865C>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3865C>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3425C>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2433C>T (CCDC180) NP_001334939.1:p.Tyr811=
NM_020893.3:c.2442C>T (CCDC180) NP_065944.2:p.Tyr814=
NM_001348010.2:c.2433C>T (CCDC180) NP_001334939.1:p.Tyr811=
NM_020893.4:c.2442C>T (CCDC180) NP_065944.2:p.Tyr814=
NM_001348010.4:c.2301C>T (CCDC180) NP_001334939.2:p.Tyr767=
NM_020893.6:c.2310C>T (CCDC180) MANE Select NP_065944.3:p.Tyr770=