Canonical Allele Identifier: CA475842732

Gene: KCNE3

Linked Data

• dbSNP Id: rs1863839552
• MyVariant Identifiers: chr11:g.74168327C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457282C>A , CM000673.2:g.74457282C>A	GRCh38
NC_000011.9:g.74168327C>A , CM000673.1:g.74168327C>A	GRCh37
NC_000011.8:g.73845975C>A	NCBI36
NG_011833.1:g.15274G>T , LRG_439:g.15274G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000310128.9:c.282G>T MANE Select	ENSP00000310557.4:p.Val94=
ENST00000310128.8:c.282G>T	ENSP00000310557.4:p.Val94=
ENST00000525550.1:c.282G>T	ENSP00000433633.1:p.Val94=
ENST00000532569.5:c.282G>T	ENSP00000431739.1:p.Val94=
NM_005472.4:c.282G>T , LRG_439t1:c.282G>T	NP_005463.1:p.Val94=
XM_011544713.1:c.414G>T	XP_011543015.1:p.Val138=
XM_011544713.2:c.414G>T	XP_011543015.1:p.Val138=
XM_017017047.1:c.282G>T	XP_016872536.1:p.Val94=
XM_017017048.1:c.282G>T	XP_016872537.1:p.Val94=
XM_017017049.1:c.282G>T	XP_016872538.1:p.Val94=
XM_017017051.2:c.282G>T	XP_016872540.1:p.Val94=
XM_017017052.1:c.282G>T	XP_016872541.1:p.Val94=
NM_005472.5:c.282G>T MANE Select	NP_005463.1:p.Val94=