Canonical Allele Identifier: CA466158386

Gene: CCDC180 SUGT1P4-STRA6LP-CCDC180

Linked Data

• MyVariant Identifiers: chr9:g.100105708C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.97343426C>T , CM000671.2:g.97343426C>T	GRCh38
NC_000009.11:g.100105708C>T , CM000671.1:g.100105708C>T	GRCh37
NC_000009.10:g.99145529C>T	NCBI36
NG_052792.1:g.41123C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529487.3:c.2361C>T (CCDC180) MANE Select	ENSP00000434727.2:p.Val787=
ENST00000460482.6:n.2695C>T (CCDC180)
ENST00000494917.6:n.2564C>T (CCDC180)
ENST00000528678.1:n.457C>T (CCDC180)
ENST00000529487.1:c.2493C>T (CCDC180)	ENSP00000434727.1:p.Val831=
ENST00000530011.1:n.236-5685C>T (CCDC180)
NM_020893.2:c.2493C>T (CCDC180)	NP_065944.2:p.Val831=
NR_036527.1:n.3916C>T (SUGT1P4-STRA6LP-CCDC180)
NR_036528.1:n.3916C>T (SUGT1P4-STRA6LP-CCDC180)
NR_036529.1:n.3476C>T (SUGT1P4-STRA6LP-CCDC180)
NM_001348010.1:c.2484C>T (CCDC180)	NP_001334939.1:p.Val828=
NM_020893.3:c.2493C>T (CCDC180)	NP_065944.2:p.Val831=
NM_001348010.2:c.2484C>T (CCDC180)	NP_001334939.1:p.Val828=
NM_020893.4:c.2493C>T (CCDC180)	NP_065944.2:p.Val831=
NM_001348010.4:c.2352C>T (CCDC180)	NP_001334939.2:p.Val784=
NM_020893.6:c.2361C>T (CCDC180) MANE Select	NP_065944.3:p.Val787=