Canonical Allele Identifier: CA374158826

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105787G>A (hg19) ; chr9:g.97343505G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343505G>A , CM000671.2:g.97343505G>A	GRCh38
NC_000009.11:g.100105787G>A , CM000671.1:g.100105787G>A	GRCh37
NC_000009.10:g.99145608G>A	NCBI36
NG_052792.1:g.41202G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2440G>A (CCDC180) MANE Select	ENSP00000434727.2:p.Ala814Thr
ENST00000460482.6:n.2774G>A (CCDC180)
ENST00000494917.6:n.2643G>A (CCDC180)
ENST00000528678.1:n.536G>A (CCDC180)
ENST00000529487.1:c.2572G>A (CCDC180)	ENSP00000434727.1:p.Ala858Thr
ENST00000530011.1:n.236-5606G>A (CCDC180)
NM_020893.2:c.2572G>A (CCDC180)	NP_065944.2:p.Ala858Thr
NR_036527.1:n.3995G>A (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3995G>A (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3555G>A (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2563G>A (CCDC180)	NP_001334939.1:p.Ala855Thr
NM_020893.3:c.2572G>A (CCDC180)	NP_065944.2:p.Ala858Thr
NM_001348010.2:c.2563G>A (CCDC180)	NP_001334939.1:p.Ala855Thr
NM_020893.4:c.2572G>A (CCDC180)	NP_065944.2:p.Ala858Thr
NM_001348010.4:c.2431G>A (CCDC180)	NP_001334939.2:p.Ala811Thr
NM_020893.6:c.2440G>A (CCDC180) MANE Select	NP_065944.3:p.Ala814Thr