Canonical Allele Identifier: CA1150264418

Gene: CCDC27

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3763712T= , CM000663.2:g.3763712T=	GRCh38
NC_000001.10:g.3680276T= , CM000663.1:g.3680276T=	GRCh37
NC_000001.9:g.3670136T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000294600.7:c.1328T= MANE Select	ENSP00000294600.2:p.Ile443=
ENST00000294600.6:c.1328T=	ENSP00000294600.2:p.Ile443=
ENST00000462521.2:c.*841T=	ENSP00000463275.1:n.*841T=
NM_152492.2:c.1328T=	NP_689705.2:p.Ile443=
XM_011540780.1:c.1328T=	XP_011539082.1:p.Ile443=
XM_011540781.1:c.1328T=	XP_011539083.1:p.Ile443=
XM_011540782.1:c.1328T=	XP_011539084.1:p.Ile443=
XM_011540783.1:c.974T=	XP_011539085.1:p.Ile325=
XR_946553.1:n.1412T=
XR_946554.1:n.1412T=
XM_017000402.1:c.1559T=	XP_016855891.1:p.Ile520=
XM_017000403.1:c.1559T=	XP_016855892.1:p.Ile520=
XM_017000404.2:c.1559T=	XP_016855893.1:p.Ile520=
XM_017000405.1:c.1559T=	XP_016855894.1:p.Ile520=
XM_017000406.1:c.1205T=	XP_016855895.1:p.Ile402=
XR_001736991.1:n.1643T=
XR_001736992.1:n.1643T=
NM_152492.3:c.1328T= MANE Select	NP_689705.2:p.Ile443=