Canonical Allele Identifier: CA374158812

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• gnomAD v4: 9-97343497-C-T
• COSMIC: COSM50587
• MyVariant Identifiers: chr9:g.100105779C>T (hg19) ; chr9:g.97343497C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343497C>T , CM000671.2:g.97343497C>T	GRCh38
NC_000009.11:g.100105779C>T , CM000671.1:g.100105779C>T	GRCh37
NC_000009.10:g.99145600C>T	NCBI36
NG_052792.1:g.41194C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2432C>T (CCDC180) MANE Select	ENSP00000434727.2:p.Thr811Ile
ENST00000460482.6:n.2766C>T (CCDC180)
ENST00000494917.6:n.2635C>T (CCDC180)
ENST00000528678.1:n.528C>T (CCDC180)
ENST00000529487.1:c.2564C>T (CCDC180)	ENSP00000434727.1:p.Thr855Ile
ENST00000530011.1:n.236-5614C>T (CCDC180)
NM_020893.2:c.2564C>T (CCDC180)	NP_065944.2:p.Thr855Ile
NR_036527.1:n.3987C>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3987C>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3547C>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2555C>T (CCDC180)	NP_001334939.1:p.Thr852Ile
NM_020893.3:c.2564C>T (CCDC180)	NP_065944.2:p.Thr855Ile
NM_001348010.2:c.2555C>T (CCDC180)	NP_001334939.1:p.Thr852Ile
NM_020893.4:c.2564C>T (CCDC180)	NP_065944.2:p.Thr855Ile
NM_001348010.4:c.2423C>T (CCDC180)	NP_001334939.2:p.Thr808Ile
NM_020893.6:c.2432C>T (CCDC180) MANE Select	NP_065944.3:p.Thr811Ile