Canonical Allele Identifier: CA1282423170

Gene: CCDC93

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.118005492G= , CM000664.2:g.118005492G=	GRCh38
NC_000002.11:g.118763068G= , CM000664.1:g.118763068G=	GRCh37
NC_000002.10:g.118479538G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376300.7:c.251+1230C= MANE Select	ENSP00000365477.2:n.251+1230C=
ENST00000319432.9:c.251+1230C=	ENSP00000324135.5:n.251+1230C=
ENST00000376300.6:c.251+1230C=	ENSP00000365477.2:n.251+1230C=
NM_019044.4:c.251+1230C=	NP_061917.3:n.251+1230C=
XM_006712600.2:c.419+1230C=	XP_006712663.1:n.419+1230C=
XM_011511359.1:c.419+1230C=	XP_011509661.1:n.419+1230C=
XM_011511360.1:c.419+1230C=	XP_011509662.1:n.419+1230C=
XM_011511361.1:c.-121-708C=	XP_011509663.1:n.-121-708C=
XM_011511362.1:c.-37+1230C=	XP_011509664.1:n.-37+1230C=
XM_011511363.1:c.419+1230C=	XP_011509665.1:n.419+1230C=
XM_011511363.2:c.419+1230C=	XP_011509665.1:n.419+1230C=
NM_019044.5:c.251+1230C= MANE Select	NP_061917.3:n.251+1230C=