Canonical Allele Identifier: CA466159343
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

dbSNP Id: rs2118779969
gnomAD v4: 9-97343558-G-A
MyVariant Identifiers: chr9:g.100105840G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343558G>A , CM000671.2:g.97343558G>A GRCh38
NC_000009.11:g.100105840G>A , CM000671.1:g.100105840G>A GRCh37
NC_000009.10:g.99145661G>A NCBI36
NG_052792.1:g.41255G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000529487.3:c.2493G>A (CCDC180) MANE Select ENSP00000434727.2:p.Lys831=
ENST00000460482.6:n.2827G>A (CCDC180)
ENST00000494917.6:n.2696G>A (CCDC180)
ENST00000528678.1:n.589G>A (CCDC180)
ENST00000529487.1:c.2625G>A (CCDC180) ENSP00000434727.1:p.Lys875=
ENST00000530011.1:n.236-5553G>A (CCDC180)
NM_020893.2:c.2625G>A (CCDC180) NP_065944.2:p.Lys875=
NR_036527.1:n.4048G>A (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4048G>A (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3608G>A (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2616G>A (CCDC180) NP_001334939.1:p.Lys872=
NM_020893.3:c.2625G>A (CCDC180) NP_065944.2:p.Lys875=
NM_001348010.2:c.2616G>A (CCDC180) NP_001334939.1:p.Lys872=
NM_020893.4:c.2625G>A (CCDC180) NP_065944.2:p.Lys875=
NM_001348010.4:c.2484G>A (CCDC180) NP_001334939.2:p.Lys828=
NM_020893.6:c.2493G>A (CCDC180) MANE Select NP_065944.3:p.Lys831=