Canonical Allele Identifier: CA1315898041

Gene: C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190120966T= , CM000664.2:g.190120966T=	GRCh38
NC_000002.11:g.190985692T= , CM000664.1:g.190985692T=	GRCh37
NC_000002.10:g.190693937T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450357.5:c.-290+29996T=	ENSP00000394370.1:n.-290+29996T=
ENST00000490033.5:n.226+25364T=
ENST00000495546.1:n.271+40943T=
XM_005246905.1:c.-290+40943T=	XP_005246962.1:n.-290+40943T=
XM_011511982.1:c.-290+29996T=	XP_011510284.1:n.-290+29996T=
XM_011511983.1:c.-290+25364T=	XP_011510285.1:n.-290+25364T=
XM_011511984.1:c.-290+25364T=	XP_011510286.1:n.-290+25364T=
XM_011511985.1:c.-290+29996T=	XP_011510287.1:n.-290+29996T=
XM_011511986.1:c.-165+40943T=	XP_011510288.1:n.-165+40943T=
XM_011511984.3:c.-290+25364T=	XP_011510286.1:n.-290+25364T=
XM_011511985.3:c.-290+29996T=	XP_011510287.1:n.-290+29996T=
XM_011511986.2:c.-165+40943T=	XP_011510288.1:n.-165+40943T=