Canonical Allele Identifier: CA11226986

Gene: EML6

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.54929493G>A , CM000664.2:g.54929493G>A	GRCh38
NC_000002.11:g.55156630G>A , CM000664.1:g.55156630G>A	GRCh37
NC_000002.10:g.55010134G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356458.8:c.4004+742G>A MANE Select	ENSP00000348842.6:n.4004+742G>A
ENST00000356458.7:c.4004+742G>A	ENSP00000348842.6:n.4004+742G>A
ENST00000673695.1:c.4004+742G>A	ENSP00000501148.1:n.4004+742G>A
ENST00000673912.1:c.4004+742G>A	ENSP00000501234.1:n.4004+742G>A
ENST00000356458.6:c.4004+742G>A	ENSP00000348842.6:n.4004+742G>A
NM_001039753.2:c.4004+742G>A	NP_001034842.2:n.4004+742G>A
XM_006712017.2:c.902+742G>A	XP_006712080.1:n.902+742G>A
XM_011532835.1:c.3278+742G>A	XP_011531137.1:n.3278+742G>A
XM_011532836.1:c.3278+742G>A	XP_011531138.1:n.3278+742G>A
XM_011532837.1:c.3278+742G>A	XP_011531139.1:n.3278+742G>A
XM_011532838.1:c.2912+742G>A	XP_011531140.1:n.2912+742G>A
XM_011532839.1:c.2813+742G>A	XP_011531141.1:n.2813+742G>A
XM_011532840.1:c.2813+742G>A	XP_011531142.1:n.2813+742G>A
XM_011532841.1:c.896+742G>A	XP_011531143.1:n.896+742G>A
XM_017004098.2:c.4004+742G>A	XP_016859587.1:n.4004+742G>A
XM_017004099.2:c.4004+742G>A	XP_016859588.1:n.4004+742G>A
XM_017004100.2:c.4004+742G>A	XP_016859589.1:n.4004+742G>A
XM_017004101.1:c.2912+742G>A	XP_016859590.1:n.2912+742G>A
NM_001039753.4:c.4004+742G>A MANE Select	NP_001034842.2:n.4004+742G>A