Canonical Allele Identifier: CA338036859

Gene: CCDC27

Linked Data

• MyVariant Identifiers: chr1:g.3680279C>G (hg19) ; chr1:g.3763715C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3763715C>G , CM000663.2:g.3763715C>G	GRCh38
NC_000001.10:g.3680279C>G , CM000663.1:g.3680279C>G	GRCh37
NC_000001.9:g.3670139C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000294600.7:c.1331C>G MANE Select	ENSP00000294600.2:p.Ala444Gly
ENST00000294600.6:c.1331C>G	ENSP00000294600.2:p.Ala444Gly
ENST00000462521.2:c.*844C>G	ENSP00000463275.1:n.*844C>G
NM_152492.2:c.1331C>G	NP_689705.2:p.Ala444Gly
XM_011540780.1:c.1331C>G	XP_011539082.1:p.Ala444Gly
XM_011540781.1:c.1331C>G	XP_011539083.1:p.Ala444Gly
XM_011540782.1:c.1331C>G	XP_011539084.1:p.Ala444Gly
XM_011540783.1:c.977C>G	XP_011539085.1:p.Ala326Gly
XR_946553.1:n.1415C>G
XR_946554.1:n.1415C>G
XM_017000402.1:c.1562C>G	XP_016855891.1:p.Ala521Gly
XM_017000403.1:c.1562C>G	XP_016855892.1:p.Ala521Gly
XM_017000404.2:c.1562C>G	XP_016855893.1:p.Ala521Gly
XM_017000405.1:c.1562C>G	XP_016855894.1:p.Ala521Gly
XM_017000406.1:c.1208C>G	XP_016855895.1:p.Ala403Gly
XR_001736991.1:n.1646C>G
XR_001736992.1:n.1646C>G
NM_152492.3:c.1331C>G MANE Select	NP_689705.2:p.Ala444Gly