Canonical Allele Identifier: CA2325368376

Gene: EPS15L1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.16437492A= , CM000681.2:g.16437492A=	GRCh38
NC_000019.9:g.16548303A= , CM000681.1:g.16548303A=	GRCh37
NC_000019.8:g.16409303A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000455140.7:c.309+278T= MANE Select	ENSP00000393313.1:n.309+278T=
ENST00000248070.10:c.309+278T=	ENSP00000248070.5:n.309+278T=
ENST00000455140.6:c.309+278T=	ENSP00000393313.1:n.309+278T=
ENST00000535753.6:c.309+278T=	ENSP00000440103.1:n.309+278T=
ENST00000592031.5:c.*46+278T=	ENSP00000465286.2:n.*46+278T=
ENST00000593760.5:c.166-3009T=	ENSP00000472958.1:n.166-3009T=
ENST00000594975.5:c.309+278T=	ENSP00000471662.1:n.309+278T=
ENST00000596037.5:c.309+278T=	ENSP00000472135.1:n.309+278T=
ENST00000597559.5:n.339+278T=
ENST00000597937.5:c.309+278T=	ENSP00000472267.1:n.309+278T=
ENST00000602022.5:c.309+278T=	ENSP00000471981.1:n.309+278T=
NM_001258374.1:c.309+278T=	NP_001245303.1:n.309+278T=
NM_001258375.1:c.309+278T=	NP_001245304.1:n.309+278T=
NM_001258376.1:c.309+278T=	NP_001245305.1:n.309+278T=
NM_021235.2:c.309+278T=	NP_067058.1:n.309+278T=
NR_047665.1:n.376+278T=
NR_047666.1:n.353+278T=
XM_017027086.2:c.309+278T=	XP_016882575.1:n.309+278T=
XM_017027087.2:c.309+278T=	XP_016882576.1:n.309+278T=
XM_017027088.2:c.309+278T=	XP_016882577.1:n.309+278T=
XM_017027089.2:c.309+278T=	XP_016882578.1:n.309+278T=
XM_017027090.2:c.309+278T=	XP_016882579.1:n.309+278T=
XM_017027091.2:c.309+278T=	XP_016882580.1:n.309+278T=
XM_017027092.2:c.309+278T=	XP_016882581.1:n.309+278T=
NM_001258374.2:c.309+278T=	NP_001245303.1:n.309+278T=
NM_001258374.3:c.309+278T= MANE Select	NP_001245303.1:n.309+278T=
NM_001258375.2:c.309+278T=	NP_001245304.1:n.309+278T=
NM_001258376.2:c.309+278T=	NP_001245305.1:n.309+278T=
NM_021235.3:c.309+278T=	NP_067058.1:n.309+278T=
NR_047665.2:n.334+278T=