Canonical Allele Identifier: CA10974729

Gene: ETNK2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204143856G>A , CM000663.2:g.204143856G>A	GRCh38
NC_000001.10:g.204112984G>A , CM000663.1:g.204112984G>A	GRCh37
NC_000001.9:g.202379607G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367202.9:c.642-2399C>T MANE Select	ENSP00000356170.4:n.642-2399C>T
ENST00000367201.7:c.642-2399C>T	ENSP00000356169.3:n.642-2399C>T
ENST00000367202.8:c.642-2399C>T	ENSP00000356170.4:n.642-2399C>T
ENST00000422699.5:c.240-2399C>T	ENSP00000405497.1:n.240-2399C>T
ENST00000444817.1:c.180-2399C>T	ENSP00000406241.1:n.180-2399C>T
ENST00000452983.5:c.213-2399C>T	ENSP00000398091.1:n.213-2399C>T
ENST00000472340.5:n.350-2399C>T
NM_001297760.1:c.642-2399C>T	NP_001284689.1:n.642-2399C>T
NM_001297761.1:c.108-2399C>T	NP_001284690.1:n.108-2399C>T
NM_001297762.1:c.519-2399C>T	NP_001284691.1:n.519-2399C>T
NM_018208.3:c.642-2399C>T	NP_060678.2:n.642-2399C>T
XM_005245303.1:c.519-2399C>T	XP_005245360.1:n.519-2399C>T
XM_011509714.1:c.108-2399C>T	XP_011508016.1:n.108-2399C>T
XM_011509715.1:c.108-2399C>T	XP_011508017.1:n.108-2399C>T
XM_011509714.2:c.108-2399C>T	XP_011508016.1:n.108-2399C>T
XM_011509715.2:c.108-2399C>T	XP_011508017.1:n.108-2399C>T
XM_017001632.1:c.108-2399C>T	XP_016857121.1:n.108-2399C>T
XM_024448127.1:c.330-2399C>T	XP_024303895.1:n.330-2399C>T
NM_018208.4:c.642-2399C>T MANE Select	NP_060678.2:n.642-2399C>T
NM_001297760.2:c.642-2399C>T	NP_001284689.1:n.642-2399C>T
NM_001297761.2:c.108-2399C>T	NP_001284690.1:n.108-2399C>T
NM_001297762.2:c.519-2399C>T	NP_001284691.1:n.519-2399C>T