Canonical Allele Identifier: CA2300590935

Gene: EPG5

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.45910737G= , CM000680.2:g.45910737G=	GRCh38
NC_000018.9:g.43490702G= , CM000680.1:g.43490702G=	GRCh37
NC_000018.8:g.41744700G=	NCBI36
NG_042838.1:g.61603C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000586655.2:n.2173C=
ENST00000587884.2:c.3989C=	ENSP00000466990.2:p.Pro1330=
ENST00000590884.6:c.3989C=	ENSP00000466403.2:p.Pro1330=
ENST00000592272.6:c.3989C=	ENSP00000467464.2:p.Pro1330=
ENST00000696482.1:c.3729C=	ENSP00000512656.1:n.3729C=
ENST00000696483.1:c.3989C=	ENSP00000512657.1:p.Pro1330=
ENST00000696484.1:c.3989C=	ENSP00000512658.1:p.Pro1330=
ENST00000696485.1:c.3989C=	ENSP00000512659.1:p.Pro1330=
ENST00000696489.1:c.3989C=	ENSP00000512660.1:p.Pro1330=
ENST00000696490.1:c.3989C=	ENSP00000512661.1:p.Pro1330=
ENST00000282041.11:c.3989C= MANE Select	ENSP00000282041.4:p.Pro1330=
ENST00000282041.9:c.3989C=	ENSP00000282041.4:p.Pro1330=
ENST00000585906.5:n.768C=
ENST00000587884.1:c.614C=	ENSP00000466990.1:p.Pro205=
ENST00000587974.1:n.4024C=
ENST00000590884.5:c.614C=	ENSP00000466403.1:p.Pro205=
ENST00000592272.5:c.614C=	ENSP00000467464.1:p.Pro205=
NM_020964.2:c.3989C=	NP_066015.2:p.Pro1330=
XM_011526120.1:c.4016C=	XP_011524422.1:p.Pro1339=
XM_011526121.1:c.4016C=	XP_011524423.1:p.Pro1339=
XM_011526122.1:c.3989C=	XP_011524424.1:p.Pro1330=
XM_011526123.1:c.4016C=	XP_011524425.1:p.Pro1339=
XM_011526124.1:c.4016C=	XP_011524426.1:p.Pro1339=
XM_011526125.1:c.3875C=	XP_011524427.1:p.Pro1292=
XM_011526126.1:c.2951C=	XP_011524428.1:p.Pro984=
XM_011526127.1:c.4016C=	XP_011524429.1:p.Pro1339=
XM_011526128.1:c.4016C=	XP_011524430.1:p.Pro1339=
XR_935244.1:n.4089C=
NM_020964.3:c.3989C= MANE Select	NP_066015.2:p.Pro1330=
XM_017025889.1:c.3989C=	XP_016881378.1:p.Pro1330=
XM_017025890.2:c.3989C=	XP_016881379.1:p.Pro1330=
XM_017025891.1:c.3848C=	XP_016881380.1:p.Pro1283=
XM_017025892.1:c.2924C=	XP_016881381.1:p.Pro975=
XM_017025893.1:c.614C=	XP_016881382.1:p.Pro205=
XR_001753256.1:n.4071C=
XR_001753257.1:n.4071C=