Canonical Allele Identifier: CA1957714054

Gene: CCDC179 GAS2

Linked Data

• dbSNP Id: rs4281481

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22859013C>A , CM000673.2:g.22859013C>A	GRCh38
NC_000011.9:g.22880559C>A , CM000673.1:g.22880559C>A	GRCh37
NC_000011.8:g.22837135C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000532798.3:c.90+439G>T (CCDC179) MANE Select	ENSP00000457511.1:n.90+439G>T
ENST00000532798.2:c.90+439G>T (CCDC179)	ENSP00000457511.1:n.90+439G>T
NM_001195637.1:c.90+439G>T (CCDC179)	NP_001182566.1:n.90+439G>T
XM_011519802.1:c.90+439G>T (CCDC179)	XP_011518104.1:n.90+439G>T
XM_011519803.1:c.90+439G>T (CCDC179)	XP_011518105.1:n.90+439G>T
XM_011519804.1:c.90+439G>T (CCDC179)	XP_011518106.1:n.90+439G>T
XR_931120.1:n.430+20649C>A
XR_931122.1:n.431-4900C>A
XR_931123.1:n.361+20649C>A
XM_011519802.2:c.90+439G>T (CCDC179)	XP_011518104.1:n.90+439G>T
XM_011519803.2:c.90+439G>T (CCDC179)	XP_011518105.1:n.90+439G>T
XR_001747829.1:n.1323+20649C>A (GAS2)
NM_001195637.2:c.90+439G>T (CCDC179) MANE Select	NP_001182566.1:n.90+439G>T