Canonical Allele Identifier: CA1315898056

Gene: C2orf88

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.190121005T= , CM000664.2:g.190121005T=	GRCh38
NC_000002.11:g.190985731T= , CM000664.1:g.190985731T=	GRCh37
NC_000002.10:g.190693976T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000450357.5:c.-290+30035T=	ENSP00000394370.1:n.-290+30035T=
ENST00000490033.5:n.226+25403T=
ENST00000495546.1:n.271+40982T=
XM_005246905.1:c.-290+40982T=	XP_005246962.1:n.-290+40982T=
XM_011511982.1:c.-290+30035T=	XP_011510284.1:n.-290+30035T=
XM_011511983.1:c.-290+25403T=	XP_011510285.1:n.-290+25403T=
XM_011511984.1:c.-290+25403T=	XP_011510286.1:n.-290+25403T=
XM_011511985.1:c.-290+30035T=	XP_011510287.1:n.-290+30035T=
XM_011511986.1:c.-165+40982T=	XP_011510288.1:n.-165+40982T=
XM_011511984.3:c.-290+25403T=	XP_011510286.1:n.-290+25403T=
XM_011511985.3:c.-290+30035T=	XP_011510287.1:n.-290+30035T=
XM_011511986.2:c.-165+40982T=	XP_011510288.1:n.-165+40982T=