Canonical Allele Identifier: CA1957713992
Gene: CCDC179 HGNC NCBI
GAS2 HGNC NCBI

Linked Data

dbSNP Id: rs1858595552

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.22858855G>C , CM000673.2:g.22858855G>C GRCh38
NC_000011.9:g.22880401G>C , CM000673.1:g.22880401G>C GRCh37
NC_000011.8:g.22836977G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000532798.3:c.90+597C>G (CCDC179) MANE Select ENSP00000457511.1:n.90+597C>G
ENST00000532798.2:c.90+597C>G (CCDC179) ENSP00000457511.1:n.90+597C>G
NM_001195637.1:c.90+597C>G (CCDC179) NP_001182566.1:n.90+597C>G
XM_011519802.1:c.90+597C>G (CCDC179) XP_011518104.1:n.90+597C>G
XM_011519803.1:c.90+597C>G (CCDC179) XP_011518105.1:n.90+597C>G
XM_011519804.1:c.90+597C>G (CCDC179) XP_011518106.1:n.90+597C>G
XR_931120.1:n.430+20491G>C
XR_931122.1:n.431-5058G>C
XR_931123.1:n.361+20491G>C
XM_011519802.2:c.90+597C>G (CCDC179) XP_011518104.1:n.90+597C>G
XM_011519803.2:c.90+597C>G (CCDC179) XP_011518105.1:n.90+597C>G
XR_001747829.1:n.1323+20491G>C (GAS2)
NM_001195637.2:c.90+597C>G (CCDC179) MANE Select NP_001182566.1:n.90+597C>G