Canonical Allele Identifier: CA1251969054

Gene: EML6

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54854239C= , CM000664.2:g.54854239C=	GRCh38
NC_000002.11:g.55081376C= , CM000664.1:g.55081376C=	GRCh37
NC_000002.10:g.54934880C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356458.8:c.1657+384C= MANE Select	ENSP00000348842.6:n.1657+384C=
ENST00000356458.7:c.1657+384C=	ENSP00000348842.6:n.1657+384C=
ENST00000673695.1:c.1657+384C=	ENSP00000501148.1:n.1657+384C=
ENST00000673912.1:c.1657+384C=	ENSP00000501234.1:n.1657+384C=
ENST00000356458.6:c.1657+384C=	ENSP00000348842.6:n.1657+384C=
ENST00000493997.1:n.5+384C=
NM_001039753.2:c.1657+384C=	NP_001034842.2:n.1657+384C=
XM_011532835.1:c.931+384C=	XP_011531137.1:n.931+384C=
XM_011532836.1:c.931+384C=	XP_011531138.1:n.931+384C=
XM_011532837.1:c.931+384C=	XP_011531139.1:n.931+384C=
XM_011532838.1:c.565+384C=	XP_011531140.1:n.565+384C=
XM_011532839.1:c.466+384C=	XP_011531141.1:n.466+384C=
XM_011532840.1:c.466+384C=	XP_011531142.1:n.466+384C=
XM_017004098.2:c.1657+384C=	XP_016859587.1:n.1657+384C=
XM_017004099.2:c.1657+384C=	XP_016859588.1:n.1657+384C=
XM_017004100.2:c.1657+384C=	XP_016859589.1:n.1657+384C=
XM_017004101.1:c.565+384C=	XP_016859590.1:n.565+384C=
XM_017004102.1:c.1657+384C=	XP_016859591.1:n.1657+384C=
XR_001738743.1:n.2481+384C=
XR_002959298.1:n.2481+384C=
NM_001039753.4:c.1657+384C= MANE Select	NP_001034842.2:n.1657+384C=