Canonical Allele Identifier: CA1866473556

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343527C= , CM000671.2:g.97343527C=	GRCh38
NC_000009.11:g.100105809C= , CM000671.1:g.100105809C=	GRCh37
NC_000009.10:g.99145630C=	NCBI36
NG_052792.1:g.41224C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2462C= (CCDC180) MANE Select	ENSP00000434727.2:p.Thr821=
ENST00000460482.6:n.2796C= (CCDC180)
ENST00000494917.6:n.2665C= (CCDC180)
ENST00000528678.1:n.558C= (CCDC180)
ENST00000529487.1:c.2594C= (CCDC180)	ENSP00000434727.1:p.Thr865=
ENST00000530011.1:n.236-5584C= (CCDC180)
NM_020893.2:c.2594C= (CCDC180)	NP_065944.2:p.Thr865=
NR_036527.1:n.4017C= (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4017C= (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3577C= (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2585C= (CCDC180)	NP_001334939.1:p.Thr862=
NM_020893.3:c.2594C= (CCDC180)	NP_065944.2:p.Thr865=
NM_001348010.2:c.2585C= (CCDC180)	NP_001334939.1:p.Thr862=
NM_020893.4:c.2594C= (CCDC180)	NP_065944.2:p.Thr865=
NM_001348010.4:c.2453C= (CCDC180)	NP_001334939.2:p.Thr818=
NM_020893.6:c.2462C= (CCDC180) MANE Select	NP_065944.3:p.Thr821=