Canonical Allele Identifier: CA374158632

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105701A>T (hg19) ; chr9:g.97343419A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343419A>T , CM000671.2:g.97343419A>T	GRCh38
NC_000009.11:g.100105701A>T , CM000671.1:g.100105701A>T	GRCh37
NC_000009.10:g.99145522A>T	NCBI36
NG_052792.1:g.41116A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2354A>T (CCDC180) MANE Select	ENSP00000434727.2:p.Tyr785Phe
ENST00000460482.6:n.2688A>T (CCDC180)
ENST00000494917.6:n.2557A>T (CCDC180)
ENST00000528678.1:n.450A>T (CCDC180)
ENST00000529487.1:c.2486A>T (CCDC180)	ENSP00000434727.1:p.Tyr829Phe
ENST00000530011.1:n.236-5692A>T (CCDC180)
NM_020893.2:c.2486A>T (CCDC180)	NP_065944.2:p.Tyr829Phe
NR_036527.1:n.3909A>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3909A>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3469A>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2477A>T (CCDC180)	NP_001334939.1:p.Tyr826Phe
NM_020893.3:c.2486A>T (CCDC180)	NP_065944.2:p.Tyr829Phe
NM_001348010.2:c.2477A>T (CCDC180)	NP_001334939.1:p.Tyr826Phe
NM_020893.4:c.2486A>T (CCDC180)	NP_065944.2:p.Tyr829Phe
NM_001348010.4:c.2345A>T (CCDC180)	NP_001334939.2:p.Tyr782Phe
NM_020893.6:c.2354A>T (CCDC180) MANE Select	NP_065944.3:p.Tyr785Phe