Canonical Allele Identifier: CA1957714064

Gene: CCDC179 GAS2

Linked Data

• dbSNP Id: rs1858601448

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22859025_22859026insA , CM000673.2:g.22859025_22859026insA	GRCh38
NC_000011.9:g.22880571_22880572insA , CM000673.1:g.22880571_22880572insA	GRCh37
NC_000011.8:g.22837147_22837148insA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532798.3:c.90+426_90+427insT (CCDC179) MANE Select	ENSP00000457511.1:n.90+426_90+427insT
ENST00000532798.2:c.90+426_90+427insT (CCDC179)	ENSP00000457511.1:n.90+426_90+427insT
NM_001195637.1:c.90+426_90+427insT (CCDC179)	NP_001182566.1:n.90+426_90+427insT
XM_011519802.1:c.90+426_90+427insT (CCDC179)	XP_011518104.1:n.90+426_90+427insT
XM_011519803.1:c.90+426_90+427insT (CCDC179)	XP_011518105.1:n.90+426_90+427insT
XM_011519804.1:c.90+426_90+427insT (CCDC179)	XP_011518106.1:n.90+426_90+427insT
XR_931120.1:n.430+20661_430+20662insA
XR_931122.1:n.431-4888_431-4887insA
XR_931123.1:n.361+20661_361+20662insA
XM_011519802.2:c.90+426_90+427insT (CCDC179)	XP_011518104.1:n.90+426_90+427insT
XM_011519803.2:c.90+426_90+427insT (CCDC179)	XP_011518105.1:n.90+426_90+427insT
XR_001747829.1:n.1323+20661_1323+20662insA (GAS2)
NM_001195637.2:c.90+426_90+427insT (CCDC179) MANE Select	NP_001182566.1:n.90+426_90+427insT