Canonical Allele Identifier: CA674741744

Gene: CCDC179 GAS2

Linked Data

• dbSNP Id: rs1281284140
• MyVariant Identifiers: chr11:g.22880499T>C (hg19) ; chr11:g.22858953T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22858953T>C , CM000673.2:g.22858953T>C	GRCh38
NC_000011.9:g.22880499T>C , CM000673.1:g.22880499T>C	GRCh37
NC_000011.8:g.22837075T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532798.3:c.90+499A>G (CCDC179) MANE Select	ENSP00000457511.1:n.90+499A>G
ENST00000532798.2:c.90+499A>G (CCDC179)	ENSP00000457511.1:n.90+499A>G
NM_001195637.1:c.90+499A>G (CCDC179)	NP_001182566.1:n.90+499A>G
XM_011519802.1:c.90+499A>G (CCDC179)	XP_011518104.1:n.90+499A>G
XM_011519803.1:c.90+499A>G (CCDC179)	XP_011518105.1:n.90+499A>G
XM_011519804.1:c.90+499A>G (CCDC179)	XP_011518106.1:n.90+499A>G
XR_931120.1:n.430+20589T>C
XR_931122.1:n.431-4960T>C
XR_931123.1:n.361+20589T>C
XM_011519802.2:c.90+499A>G (CCDC179)	XP_011518104.1:n.90+499A>G
XM_011519803.2:c.90+499A>G (CCDC179)	XP_011518105.1:n.90+499A>G
XR_001747829.1:n.1323+20589T>C (GAS2)
NM_001195637.2:c.90+499A>G (CCDC179) MANE Select	NP_001182566.1:n.90+499A>G