Canonical Allele Identifier: CA374158880

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105809C>G (hg19) ; chr9:g.97343527C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000529487.3:c.2462C>G (CCDC180) MANE Select	ENSP00000434727.2:p.Thr821Arg
ENST00000460482.6:n.2796C>G (CCDC180)
ENST00000494917.6:n.2665C>G (CCDC180)
ENST00000528678.1:n.558C>G (CCDC180)
ENST00000529487.1:c.2594C>G (CCDC180)	ENSP00000434727.1:p.Thr865Arg
ENST00000530011.1:n.236-5584C>G (CCDC180)
NM_020893.2:c.2594C>G (CCDC180)	NP_065944.2:p.Thr865Arg
NR_036527.1:n.4017C>G (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4017C>G (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3577C>G (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2585C>G (CCDC180)	NP_001334939.1:p.Thr862Arg
NM_020893.3:c.2594C>G (CCDC180)	NP_065944.2:p.Thr865Arg
NM_001348010.2:c.2585C>G (CCDC180)	NP_001334939.1:p.Thr862Arg
NM_020893.4:c.2594C>G (CCDC180)	NP_065944.2:p.Thr865Arg
NM_001348010.4:c.2453C>G (CCDC180)	NP_001334939.2:p.Thr818Arg
NM_020893.6:c.2462C>G (CCDC180) MANE Select	NP_065944.3:p.Thr821Arg