Canonical Allele Identifier: CA338036848

Gene: CCDC27

Linked Data

• MyVariant Identifiers: chr1:g.3680277T>G (hg19) ; chr1:g.3763713T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.3763713T>G , CM000663.2:g.3763713T>G	GRCh38
NC_000001.10:g.3680277T>G , CM000663.1:g.3680277T>G	GRCh37
NC_000001.9:g.3670137T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000294600.7:c.1329T>G MANE Select	ENSP00000294600.2:p.Ile443Met
ENST00000294600.6:c.1329T>G	ENSP00000294600.2:p.Ile443Met
ENST00000462521.2:c.*842T>G	ENSP00000463275.1:n.*842T>G
NM_152492.2:c.1329T>G	NP_689705.2:p.Ile443Met
XM_011540780.1:c.1329T>G	XP_011539082.1:p.Ile443Met
XM_011540781.1:c.1329T>G	XP_011539083.1:p.Ile443Met
XM_011540782.1:c.1329T>G	XP_011539084.1:p.Ile443Met
XM_011540783.1:c.975T>G	XP_011539085.1:p.Ile325Met
XR_946553.1:n.1413T>G
XR_946554.1:n.1413T>G
XM_017000402.1:c.1560T>G	XP_016855891.1:p.Ile520Met
XM_017000403.1:c.1560T>G	XP_016855892.1:p.Ile520Met
XM_017000404.2:c.1560T>G	XP_016855893.1:p.Ile520Met
XM_017000405.1:c.1560T>G	XP_016855894.1:p.Ile520Met
XM_017000406.1:c.1206T>G	XP_016855895.1:p.Ile402Met
XR_001736991.1:n.1644T>G
XR_001736992.1:n.1644T>G
NM_152492.3:c.1329T>G MANE Select	NP_689705.2:p.Ile443Met