Canonical Allele Identifier: CA2154878653

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91313319_91313322delinsCCTT , CM000676.2:g.91313319_91313322delinsCCTT	GRCh38
NC_000014.8:g.91779663_91779666delinsCCTT , CM000676.1:g.91779663_91779666delinsCCTT	GRCh37
NC_000014.7:g.90849416_90849419delinsCCTT	NCBI36
NG_033118.1:g.109523_109526delinsAAGG
NG_033118.2:g.109523_109526delinsAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389857.11:c.2494_2497delinsAAGG MANE Select	ENSP00000374507.6:p.Lys832=
ENST00000389857.10:c.2494_2497delinsAAGG	ENSP00000374507.6:p.Lys832=
NM_001080414.3:c.2494_2497delinsAAGG	NP_001073883.2:p.Lys832=
XM_005267691.3:c.2494_2497delinsAAGG	XP_005267748.1:p.Lys832=
XM_011536796.1:c.2386_2389delinsAAGG	XP_011535098.1:p.Lys796=
XR_429316.2:n.2622_2625delinsAAGG
XR_943459.1:n.2622_2625delinsAAGG
XM_005267691.5:c.2494_2497delinsAAGG	XP_005267748.1:p.Lys832=
XM_011536796.2:c.2386_2389delinsAAGG	XP_011535098.1:p.Lys796=
XM_017021335.2:c.2494_2497delinsAAGG	XP_016876824.1:p.Lys832=
XM_017021337.2:c.2494_2497delinsAAGG	XP_016876826.1:p.Lys832=
XR_429316.4:n.2620_2623delinsAAGG
NM_001080414.4:c.2494_2497delinsAAGG MANE Select	NP_001073883.2:p.Lys832=