Canonical Allele Identifier: CA2325331098

Gene: EPS15L1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.16356878G= , CM000681.2:g.16356878G=	GRCh38
NC_000019.9:g.16467689G= , CM000681.1:g.16467689G=	GRCh37
NC_000019.8:g.16328689G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455140.7:c.2587-1027C= MANE Select	ENSP00000393313.1:n.2587-1027C=
ENST00000455140.6:c.2587-1027C=	ENSP00000393313.1:n.2587-1027C=
ENST00000594851.5:c.69-1027C=
ENST00000602022.5:c.*189-1027C=	ENSP00000471981.1:n.*189-1027C=
NM_001258374.1:c.2587-1027C=	NP_001245303.1:n.2587-1027C=
NR_047665.1:n.2521-1027C=
XM_017027086.2:c.2635-1027C=	XP_016882575.1:n.2635-1027C=
XM_017027087.2:c.*34C=	XP_016882576.1:n.*34C=
XM_017027088.2:c.*50C=	XP_016882577.1:n.*50C=
XM_017027089.2:c.2528-1027C=	XP_016882578.1:n.2528-1027C=
XM_017027090.2:c.2248-1027C=	XP_016882579.1:n.2248-1027C=
XM_017027091.2:c.2381-1027C=	XP_016882580.1:n.2381-1027C=
NM_001258374.2:c.2587-1027C=	NP_001245303.1:n.2587-1027C=
NM_001258374.3:c.2587-1027C= MANE Select	NP_001245303.1:n.2587-1027C=
NR_047665.2:n.2479-1027C=