Canonical Allele Identifier: CA374158948

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105842A>C (hg19) ; chr9:g.97343560A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343560A>C , CM000671.2:g.97343560A>C	GRCh38
NC_000009.11:g.100105842A>C , CM000671.1:g.100105842A>C	GRCh37
NC_000009.10:g.99145663A>C	NCBI36
NG_052792.1:g.41257A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2495A>C (CCDC180) MANE Select	ENSP00000434727.2:p.Lys832Thr
ENST00000460482.6:n.2829A>C (CCDC180)
ENST00000494917.6:n.2698A>C (CCDC180)
ENST00000528678.1:n.591A>C (CCDC180)
ENST00000529487.1:c.2627A>C (CCDC180)	ENSP00000434727.1:p.Lys876Thr
ENST00000530011.1:n.236-5551A>C (CCDC180)
NM_020893.2:c.2627A>C (CCDC180)	NP_065944.2:p.Lys876Thr
NR_036527.1:n.4050A>C (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4050A>C (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3610A>C (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2618A>C (CCDC180)	NP_001334939.1:p.Lys873Thr
NM_020893.3:c.2627A>C (CCDC180)	NP_065944.2:p.Lys876Thr
NM_001348010.2:c.2618A>C (CCDC180)	NP_001334939.1:p.Lys873Thr
NM_020893.4:c.2627A>C (CCDC180)	NP_065944.2:p.Lys876Thr
NM_001348010.4:c.2486A>C (CCDC180)	NP_001334939.2:p.Lys829Thr
NM_020893.6:c.2495A>C (CCDC180) MANE Select	NP_065944.3:p.Lys832Thr