Canonical Allele Identifier: CA466159228
Gene: CCDC180 HGNC NCBI
SUGT1P4-STRA6LP-CCDC180 HGNC NCBI

Linked Data

gnomAD v4: 9-97343525-G-T
MyVariant Identifiers: chr9:g.100105807G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.97343525G>T , CM000671.2:g.97343525G>T GRCh38
NC_000009.11:g.100105807G>T , CM000671.1:g.100105807G>T GRCh37
NC_000009.10:g.99145628G>T NCBI36
NG_052792.1:g.41222G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000529487.3:c.2460G>T (CCDC180) MANE Select ENSP00000434727.2:p.Val820=
ENST00000460482.6:n.2794G>T (CCDC180)
ENST00000494917.6:n.2663G>T (CCDC180)
ENST00000528678.1:n.556G>T (CCDC180)
ENST00000529487.1:c.2592G>T (CCDC180) ENSP00000434727.1:p.Val864=
ENST00000530011.1:n.236-5586G>T (CCDC180)
NM_020893.2:c.2592G>T (CCDC180) NP_065944.2:p.Val864=
NR_036527.1:n.4015G>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.4015G>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3575G>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2583G>T (CCDC180) NP_001334939.1:p.Val861=
NM_020893.3:c.2592G>T (CCDC180) NP_065944.2:p.Val864=
NM_001348010.2:c.2583G>T (CCDC180) NP_001334939.1:p.Val861=
NM_020893.4:c.2592G>T (CCDC180) NP_065944.2:p.Val864=
NM_001348010.4:c.2451G>T (CCDC180) NP_001334939.2:p.Val817=
NM_020893.6:c.2460G>T (CCDC180) MANE Select NP_065944.3:p.Val820=