Canonical Allele Identifier: CA466159238

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105810A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343528A>T , CM000671.2:g.97343528A>T	GRCh38
NC_000009.11:g.100105810A>T , CM000671.1:g.100105810A>T	GRCh37
NC_000009.10:g.99145631A>T	NCBI36
NG_052792.1:g.41225A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2463A>T (CCDC180) MANE Select	ENSP00000434727.2:p.Thr821=
ENST00000460482.6:n.2797A>T (CCDC180)
ENST00000494917.6:n.2666A>T (CCDC180)
ENST00000528678.1:n.559A>T (CCDC180)
ENST00000529487.1:c.2595A>T (CCDC180)	ENSP00000434727.1:p.Thr865=
ENST00000530011.1:n.236-5583A>T (CCDC180)
NM_020893.2:c.2595A>T (CCDC180)	NP_065944.2:p.Thr865=
NR_036527.1:n.4018A>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4018A>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3578A>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2586A>T (CCDC180)	NP_001334939.1:p.Thr862=
NM_020893.3:c.2595A>T (CCDC180)	NP_065944.2:p.Thr865=
NM_001348010.2:c.2586A>T (CCDC180)	NP_001334939.1:p.Thr862=
NM_020893.4:c.2595A>T (CCDC180)	NP_065944.2:p.Thr865=
NM_001348010.4:c.2454A>T (CCDC180)	NP_001334939.2:p.Thr818=
NM_020893.6:c.2463A>T (CCDC180) MANE Select	NP_065944.3:p.Thr821=