Canonical Allele Identifier: CA2066921112

Gene: CCDC60

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.119380704A= , CM000674.2:g.119380704A=	GRCh38
NC_000012.11:g.119818509A= , CM000674.1:g.119818509A=	GRCh37
NC_000012.10:g.118302892A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000327554.3:c.90+45438A= MANE Select	ENSP00000333374.2:n.90+45438A=
ENST00000327554.2:c.90+45438A=	ENSP00000333374.2:n.90+45438A=
ENST00000535685.1:n.56+45438A=
ENST00000536742.5:c.90+45438A=	ENSP00000445505.1:n.90+45438A=
ENST00000539847.1:c.90+45438A=	ENSP00000443403.1:n.90+45438A=
ENST00000546345.5:n.240+45438A=
NM_178499.4:c.90+45438A=	NP_848594.2:n.90+45438A=
XM_011538002.1:c.90+45438A=	XP_011536304.1:n.90+45438A=
XM_011538003.1:c.90+45438A=	XP_011536305.1:n.90+45438A=
XR_944504.1:n.338+45438A=
XM_017018911.2:c.90+45438A=	XP_016874400.1:n.90+45438A=
XM_017018912.2:c.90+45438A=	XP_016874401.1:n.90+45438A=
XM_017018913.2:c.90+45438A=	XP_016874402.1:n.90+45438A=
XR_944504.2:n.536+45438A=
NM_178499.5:c.90+45438A= MANE Select	NP_848594.2:n.90+45438A=