Canonical Allele Identifier: CA2154901027

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91305633_91305634delinsAC , CM000676.2:g.91305633_91305634delinsAC	GRCh38
NC_000014.8:g.91771977_91771978delinsAC , CM000676.1:g.91771977_91771978delinsAC	GRCh37
NC_000014.7:g.90841730_90841731delinsAC	NCBI36
NG_033118.1:g.117211_117212delinsGT
NG_033118.2:g.117211_117212delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.3357+131_3357+132delinsGT MANE Select	ENSP00000374507.6:n.3357+131_3357+132delinsGT
ENST00000389857.10:c.3357+131_3357+132delinsGT	ENSP00000374507.6:n.3357+131_3357+132delinsGT
NM_001080414.3:c.3357+131_3357+132delinsGT	NP_001073883.2:n.3357+131_3357+132delinsGT
XM_005267691.3:c.3357+131_3357+132delinsGT	XP_005267748.1:n.3357+131_3357+132delinsGT
XM_011536796.1:c.3249+131_3249+132delinsGT	XP_011535098.1:n.3249+131_3249+132delinsGT
XR_429316.2:n.3485+131_3485+132delinsGT
XR_943459.1:n.3485+131_3485+132delinsGT
XM_005267691.5:c.3357+131_3357+132delinsGT	XP_005267748.1:n.3357+131_3357+132delinsGT
XM_011536796.2:c.3249+131_3249+132delinsGT	XP_011535098.1:n.3249+131_3249+132delinsGT
XM_017021335.2:c.3357+131_3357+132delinsGT	XP_016876824.1:n.3357+131_3357+132delinsGT
XM_017021336.1:c.438+131_438+132delinsGT	XP_016876825.1:n.438+131_438+132delinsGT
XR_429316.4:n.3483+131_3483+132delinsGT
NM_001080414.4:c.3357+131_3357+132delinsGT MANE Select	NP_001073883.2:n.3357+131_3357+132delinsGT