Canonical Allele Identifier: CA1866473474

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343429T= , CM000671.2:g.97343429T=	GRCh38
NC_000009.11:g.100105711T= , CM000671.1:g.100105711T=	GRCh37
NC_000009.10:g.99145532T=	NCBI36
NG_052792.1:g.41126T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2364T= (CCDC180) MANE Select	ENSP00000434727.2:p.Phe788=
ENST00000460482.6:n.2698T= (CCDC180)
ENST00000494917.6:n.2567T= (CCDC180)
ENST00000528678.1:n.460T= (CCDC180)
ENST00000529487.1:c.2496T= (CCDC180)	ENSP00000434727.1:p.Phe832=
ENST00000530011.1:n.236-5682T= (CCDC180)
NM_020893.2:c.2496T= (CCDC180)	NP_065944.2:p.Phe832=
NR_036527.1:n.3919T= (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3919T= (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3479T= (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2487T= (CCDC180)	NP_001334939.1:p.Phe829=
NM_020893.3:c.2496T= (CCDC180)	NP_065944.2:p.Phe832=
NM_001348010.2:c.2487T= (CCDC180)	NP_001334939.1:p.Phe829=
NM_020893.4:c.2496T= (CCDC180)	NP_065944.2:p.Phe832=
NM_001348010.4:c.2355T= (CCDC180)	NP_001334939.2:p.Phe785=
NM_020893.6:c.2364T= (CCDC180) MANE Select	NP_065944.3:p.Phe788=