Canonical Allele Identifier: CA374158627

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105698C>A (hg19) ; chr9:g.97343416C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343416C>A , CM000671.2:g.97343416C>A	GRCh38
NC_000009.11:g.100105698C>A , CM000671.1:g.100105698C>A	GRCh37
NC_000009.10:g.99145519C>A	NCBI36
NG_052792.1:g.41113C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2351C>A (CCDC180) MANE Select	ENSP00000434727.2:p.Thr784Asn
ENST00000460482.6:n.2685C>A (CCDC180)
ENST00000494917.6:n.2554C>A (CCDC180)
ENST00000528678.1:n.447C>A (CCDC180)
ENST00000529487.1:c.2483C>A (CCDC180)	ENSP00000434727.1:p.Thr828Asn
ENST00000530011.1:n.236-5695C>A (CCDC180)
NM_020893.2:c.2483C>A (CCDC180)	NP_065944.2:p.Thr828Asn
NR_036527.1:n.3906C>A (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3906C>A (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3466C>A (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2474C>A (CCDC180)	NP_001334939.1:p.Thr825Asn
NM_020893.3:c.2483C>A (CCDC180)	NP_065944.2:p.Thr828Asn
NM_001348010.2:c.2474C>A (CCDC180)	NP_001334939.1:p.Thr825Asn
NM_020893.4:c.2483C>A (CCDC180)	NP_065944.2:p.Thr828Asn
NM_001348010.4:c.2342C>A (CCDC180)	NP_001334939.2:p.Thr781Asn
NM_020893.6:c.2351C>A (CCDC180) MANE Select	NP_065944.3:p.Thr784Asn