Canonical Allele Identifier: CA5145540
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

dbSNP Id: rs377441754
gnomAD v3: 9-97343294-T-C
gnomAD v4: 9-97343294-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343294T>C , CM000671.2:g.97343294T>C GRCh38
NC_000009.11:g.100105576T>C , CM000671.1:g.100105576T>C GRCh37
NC_000009.10:g.99145397T>C NCBI36
NG_052792.1:g.40991T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000529487.3:c.2275-46T>C (CCDC180) MANE Select ENSP00000434727.2:n.2275-46T>C
ENST00000460482.6:n.2609-46T>C (CCDC180)
ENST00000494917.6:n.2478-46T>C (CCDC180)
ENST00000528678.1:n.371-46T>C (CCDC180)
ENST00000529487.1:c.2407-46T>C (CCDC180) ENSP00000434727.1:n.2407-46T>C
ENST00000530011.1:n.236-5817T>C (CCDC180)
NM_020893.2:c.2407-46T>C (CCDC180) NP_065944.2:n.2407-46T>C
NR_036527.1:n.3830-46T>C (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3830-46T>C (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3390-46T>C (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2398-46T>C (CCDC180) NP_001334939.1:n.2398-46T>C
NM_020893.3:c.2407-46T>C (CCDC180) NP_065944.2:n.2407-46T>C
NM_001348010.2:c.2398-46T>C (CCDC180) NP_001334939.1:n.2398-46T>C
NM_020893.4:c.2407-46T>C (CCDC180) NP_065944.2:n.2407-46T>C
NM_001348010.4:c.2266-46T>C (CCDC180) NP_001334939.2:n.2266-46T>C
NM_020893.6:c.2275-46T>C (CCDC180) MANE Select NP_065944.3:n.2275-46T>C