Canonical Allele Identifier: CA2690872658

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• gnomAD v4: 9-97343299-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343299T>A , CM000671.2:g.97343299T>A	GRCh38
NC_000009.11:g.100105581T>A , CM000671.1:g.100105581T>A	GRCh37
NC_000009.10:g.99145402T>A	NCBI36
NG_052792.1:g.40996T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2275-41T>A (CCDC180) MANE Select	ENSP00000434727.2:n.2275-41T>A
ENST00000460482.6:n.2609-41T>A (CCDC180)
ENST00000494917.6:n.2478-41T>A (CCDC180)
ENST00000528678.1:n.371-41T>A (CCDC180)
ENST00000529487.1:c.2407-41T>A (CCDC180)	ENSP00000434727.1:n.2407-41T>A
ENST00000530011.1:n.236-5812T>A (CCDC180)
NM_020893.2:c.2407-41T>A (CCDC180)	NP_065944.2:n.2407-41T>A
NR_036527.1:n.3830-41T>A (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3830-41T>A (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3390-41T>A (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2398-41T>A (CCDC180)	NP_001334939.1:n.2398-41T>A
NM_020893.3:c.2407-41T>A (CCDC180)	NP_065944.2:n.2407-41T>A
NM_001348010.2:c.2398-41T>A (CCDC180)	NP_001334939.1:n.2398-41T>A
NM_020893.4:c.2407-41T>A (CCDC180)	NP_065944.2:n.2407-41T>A
NM_001348010.4:c.2266-41T>A (CCDC180)	NP_001334939.2:n.2266-41T>A
NM_020893.6:c.2275-41T>A (CCDC180) MANE Select	NP_065944.3:n.2275-41T>A