Canonical Allele Identifier: CA374158549

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105664G>T (hg19) ; chr9:g.97343382G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343382G>T , CM000671.2:g.97343382G>T	GRCh38
NC_000009.11:g.100105664G>T , CM000671.1:g.100105664G>T	GRCh37
NC_000009.10:g.99145485G>T	NCBI36
NG_052792.1:g.41079G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2317G>T (CCDC180) MANE Select	ENSP00000434727.2:p.Asp773Tyr
ENST00000460482.6:n.2651G>T (CCDC180)
ENST00000494917.6:n.2520G>T (CCDC180)
ENST00000528678.1:n.413G>T (CCDC180)
ENST00000529487.1:c.2449G>T (CCDC180)	ENSP00000434727.1:p.Asp817Tyr
ENST00000530011.1:n.236-5729G>T (CCDC180)
NM_020893.2:c.2449G>T (CCDC180)	NP_065944.2:p.Asp817Tyr
NR_036527.1:n.3872G>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3872G>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3432G>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2440G>T (CCDC180)	NP_001334939.1:p.Asp814Tyr
NM_020893.3:c.2449G>T (CCDC180)	NP_065944.2:p.Asp817Tyr
NM_001348010.2:c.2440G>T (CCDC180)	NP_001334939.1:p.Asp814Tyr
NM_020893.4:c.2449G>T (CCDC180)	NP_065944.2:p.Asp817Tyr
NM_001348010.4:c.2308G>T (CCDC180)	NP_001334939.2:p.Asp770Tyr
NM_020893.6:c.2317G>T (CCDC180) MANE Select	NP_065944.3:p.Asp773Tyr