Canonical Allele Identifier: CA2504005701

Gene: CCDC179 GAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22859082A>T , CM000673.2:g.22859082A>T	GRCh38
NC_000011.9:g.22880628A>T , CM000673.1:g.22880628A>T	GRCh37
NC_000011.8:g.22837204A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532798.3:c.90+370T>A (CCDC179) MANE Select	ENSP00000457511.1:n.90+370T>A
ENST00000532798.2:c.90+370T>A (CCDC179)	ENSP00000457511.1:n.90+370T>A
NM_001195637.1:c.90+370T>A (CCDC179)	NP_001182566.1:n.90+370T>A
XM_011519802.1:c.90+370T>A (CCDC179)	XP_011518104.1:n.90+370T>A
XM_011519803.1:c.90+370T>A (CCDC179)	XP_011518105.1:n.90+370T>A
XM_011519804.1:c.90+370T>A (CCDC179)	XP_011518106.1:n.90+370T>A
XR_931120.1:n.430+20718A>T
XR_931122.1:n.431-4831A>T
XR_931123.1:n.361+20718A>T
XM_011519802.2:c.90+370T>A (CCDC179)	XP_011518104.1:n.90+370T>A
XM_011519803.2:c.90+370T>A (CCDC179)	XP_011518105.1:n.90+370T>A
XR_001747829.1:n.1323+20718A>T (GAS2)
NM_001195637.2:c.90+370T>A (CCDC179) MANE Select	NP_001182566.1:n.90+370T>A