Canonical Allele Identifier: CA374158862

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105801A>T (hg19) ; chr9:g.97343519A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343519A>T , CM000671.2:g.97343519A>T	GRCh38
NC_000009.11:g.100105801A>T , CM000671.1:g.100105801A>T	GRCh37
NC_000009.10:g.99145622A>T	NCBI36
NG_052792.1:g.41216A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2454A>T (CCDC180) MANE Select	ENSP00000434727.2:p.Glu818Asp
ENST00000460482.6:n.2788A>T (CCDC180)
ENST00000494917.6:n.2657A>T (CCDC180)
ENST00000528678.1:n.550A>T (CCDC180)
ENST00000529487.1:c.2586A>T (CCDC180)	ENSP00000434727.1:p.Glu862Asp
ENST00000530011.1:n.236-5592A>T (CCDC180)
NM_020893.2:c.2586A>T (CCDC180)	NP_065944.2:p.Glu862Asp
NR_036527.1:n.4009A>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4009A>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3569A>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2577A>T (CCDC180)	NP_001334939.1:p.Glu859Asp
NM_020893.3:c.2586A>T (CCDC180)	NP_065944.2:p.Glu862Asp
NM_001348010.2:c.2577A>T (CCDC180)	NP_001334939.1:p.Glu859Asp
NM_020893.4:c.2586A>T (CCDC180)	NP_065944.2:p.Glu862Asp
NM_001348010.4:c.2445A>T (CCDC180)	NP_001334939.2:p.Glu815Asp
NM_020893.6:c.2454A>T (CCDC180) MANE Select	NP_065944.3:p.Glu818Asp