Canonical Allele Identifier: CA374158840

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105793T>A (hg19) ; chr9:g.97343511T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343511T>A , CM000671.2:g.97343511T>A	GRCh38
NC_000009.11:g.100105793T>A , CM000671.1:g.100105793T>A	GRCh37
NC_000009.10:g.99145614T>A	NCBI36
NG_052792.1:g.41208T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000529487.3:c.2446T>A (CCDC180) MANE Select	ENSP00000434727.2:p.Phe816Ile
ENST00000460482.6:n.2780T>A (CCDC180)
ENST00000494917.6:n.2649T>A (CCDC180)
ENST00000528678.1:n.542T>A (CCDC180)
ENST00000529487.1:c.2578T>A (CCDC180)	ENSP00000434727.1:p.Phe860Ile
ENST00000530011.1:n.236-5600T>A (CCDC180)
NM_020893.2:c.2578T>A (CCDC180)	NP_065944.2:p.Phe860Ile
NR_036527.1:n.4001T>A (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4001T>A (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3561T>A (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2569T>A (CCDC180)	NP_001334939.1:p.Phe857Ile
NM_020893.3:c.2578T>A (CCDC180)	NP_065944.2:p.Phe860Ile
NM_001348010.2:c.2569T>A (CCDC180)	NP_001334939.1:p.Phe857Ile
NM_020893.4:c.2578T>A (CCDC180)	NP_065944.2:p.Phe860Ile
NM_001348010.4:c.2437T>A (CCDC180)	NP_001334939.2:p.Phe813Ile
NM_020893.6:c.2446T>A (CCDC180) MANE Select	NP_065944.3:p.Phe816Ile