Canonical Allele Identifier: CA2154909442

Gene: CCDC88C

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91279212A= , CM000676.2:g.91279212A=	GRCh38
NC_000014.8:g.91745556A= , CM000676.1:g.91745556A=	GRCh37
NC_000014.7:g.90815309A=	NCBI36
NG_033118.1:g.143633T=
NG_033118.2:g.143633T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389857.11:c.4768+26T= MANE Select	ENSP00000374507.6:n.4768+26T=
ENST00000331194.8:c.340+26T=	ENSP00000330332.8:n.340+26T=
ENST00000334448.5:n.580+26T=
ENST00000389857.10:c.4768+26T=	ENSP00000374507.6:n.4768+26T=
ENST00000556726.5:c.996+26T=
ENST00000557455.1:n.740+26T=
NM_001080414.3:c.4768+26T=	NP_001073883.2:n.4768+26T=
XM_011536796.1:c.4660+26T=	XP_011535098.1:n.4660+26T=
XR_429316.2:n.5043+26T=
XM_011536796.2:c.4660+26T=	XP_011535098.1:n.4660+26T=
XM_017021336.1:c.1849+26T=	XP_016876825.1:n.1849+26T=
XR_429316.4:n.5041+26T=
NM_001080414.4:c.4768+26T= MANE Select	NP_001073883.2:n.4768+26T=