Canonical Allele Identifier: CA5145594
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

dbSNP Id: rs768406843
gnomAD v3: 9-97343615-A-G
gnomAD v4: 9-97343615-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343615A>G , CM000671.2:g.97343615A>G GRCh38
NC_000009.11:g.100105897A>G , CM000671.1:g.100105897A>G GRCh37
NC_000009.10:g.99145718A>G NCBI36
NG_052792.1:g.41312A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000529487.3:c.2498+52A>G (CCDC180) MANE Select ENSP00000434727.2:n.2498+52A>G
ENST00000460482.6:n.2832+52A>G (CCDC180)
ENST00000494917.6:n.2753A>G (CCDC180)
ENST00000528678.1:n.594+52A>G (CCDC180)
ENST00000529487.1:c.2630+52A>G (CCDC180) ENSP00000434727.1:n.2630+52A>G
ENST00000530011.1:n.236-5496A>G (CCDC180)
NM_020893.2:c.2630+52A>G (CCDC180) NP_065944.2:n.2630+52A>G
NR_036527.1:n.4053+52A>G (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4053+52A>G (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3613+52A>G (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2621+52A>G (CCDC180) NP_001334939.1:n.2621+52A>G
NM_020893.3:c.2630+52A>G (CCDC180) NP_065944.2:n.2630+52A>G
NM_001348010.2:c.2621+52A>G (CCDC180) NP_001334939.1:n.2621+52A>G
NM_020893.4:c.2630+52A>G (CCDC180) NP_065944.2:n.2630+52A>G
NM_001348010.4:c.2489+52A>G (CCDC180) NP_001334939.2:n.2489+52A>G
NM_020893.6:c.2498+52A>G (CCDC180) MANE Select NP_065944.3:n.2498+52A>G