Canonical Allele Identifier: CA466158428

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105717C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343435C>A , CM000671.2:g.97343435C>A	GRCh38
NC_000009.11:g.100105717C>A , CM000671.1:g.100105717C>A	GRCh37
NC_000009.10:g.99145538C>A	NCBI36
NG_052792.1:g.41132C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2370C>A (CCDC180) MANE Select	ENSP00000434727.2:p.Pro790=
ENST00000460482.6:n.2704C>A (CCDC180)
ENST00000494917.6:n.2573C>A (CCDC180)
ENST00000528678.1:n.466C>A (CCDC180)
ENST00000529487.1:c.2502C>A (CCDC180)	ENSP00000434727.1:p.Pro834=
ENST00000530011.1:n.236-5676C>A (CCDC180)
NM_020893.2:c.2502C>A (CCDC180)	NP_065944.2:p.Pro834=
NR_036527.1:n.3925C>A (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3925C>A (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3485C>A (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2493C>A (CCDC180)	NP_001334939.1:p.Pro831=
NM_020893.3:c.2502C>A (CCDC180)	NP_065944.2:p.Pro834=
NM_001348010.2:c.2493C>A (CCDC180)	NP_001334939.1:p.Pro831=
NM_020893.4:c.2502C>A (CCDC180)	NP_065944.2:p.Pro834=
NM_001348010.4:c.2361C>A (CCDC180)	NP_001334939.2:p.Pro787=
NM_020893.6:c.2370C>A (CCDC180) MANE Select	NP_065944.3:p.Pro790=