Canonical Allele Identifier: CA2011520692

Gene: CCDC77

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.442384G= , CM000674.2:g.442384G=	GRCh38
NC_000012.11:g.551550G= , CM000674.1:g.551550G=	GRCh37
NC_000012.10:g.421811G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032358.4:c.*464G= MANE Select	NP_115734.1:n.*464G=
ENST00000239830.9:c.*464G= MANE Select	ENSP00000239830.4:n.*464G=
NM_001130146.1:c.*464G=	NP_001123618.1:n.*464G=
NM_001130146.2:c.*464G=	NP_001123618.1:n.*464G=
NM_001130147.1:c.*464G=	NP_001123619.1:n.*464G=
NM_001130147.2:c.*464G=	NP_001123619.1:n.*464G=
NM_001130148.1:c.*464G=	NP_001123620.1:n.*464G=
NM_001130148.2:c.*464G=	NP_001123620.1:n.*464G=
NM_032358.3:c.*464G=	NP_115734.1:n.*464G=
ENST00000239830.8:c.*464G=	ENSP00000239830.4:n.*464G=
ENST00000412006.6:c.*464G=	ENSP00000412925.2:n.*464G=
ENST00000422000.5:c.*464G=	ENSP00000391870.1:n.*464G=
ENST00000537286.1:n.705G=