Canonical Allele Identifier: CA674741759

Gene: CCDC179 GAS2

Linked Data

• dbSNP Id: rs1157615105
• gnomAD v3: 11-22858971-TTG-T
• gnomAD v4: 11-22858971-TTG-T
• MyVariant Identifiers: chr11:g.22880518_22880519del (hg19) ; chr11:g.22858972_22858973del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.22858976_22858977del , CM000673.2:g.22858976_22858977del	GRCh38
NC_000011.9:g.22880522_22880523del , CM000673.1:g.22880522_22880523del	GRCh37
NC_000011.8:g.22837098_22837099del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000532798.3:c.90+479_90+480del (CCDC179) MANE Select	ENSP00000457511.1:n.90+479_90+480del
ENST00000532798.2:c.90+479_90+480del (CCDC179)	ENSP00000457511.1:n.90+479_90+480del
NM_001195637.1:c.90+479_90+480del (CCDC179)	NP_001182566.1:n.90+479_90+480del
XM_011519802.1:c.90+479_90+480del (CCDC179)	XP_011518104.1:n.90+479_90+480del
XM_011519803.1:c.90+479_90+480del (CCDC179)	XP_011518105.1:n.90+479_90+480del
XM_011519804.1:c.90+479_90+480del (CCDC179)	XP_011518106.1:n.90+479_90+480del
XR_931120.1:n.430+20612_430+20613del
XR_931122.1:n.431-4937_431-4936del
XR_931123.1:n.361+20612_361+20613del
XM_011519802.2:c.90+479_90+480del (CCDC179)	XP_011518104.1:n.90+479_90+480del
XM_011519803.2:c.90+479_90+480del (CCDC179)	XP_011518105.1:n.90+479_90+480del
XR_001747829.1:n.1323+20612_1323+20613del (GAS2)
NM_001195637.2:c.90+479_90+480del (CCDC179) MANE Select	NP_001182566.1:n.90+479_90+480del