Canonical Allele Identifier: CA381974072

Gene: KCNE3

Linked Data

• MyVariant Identifiers: chr11:g.74168512G>T (hg19) ; chr11:g.74457467G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457467G>T , CM000673.2:g.74457467G>T	GRCh38
NC_000011.9:g.74168512G>T , CM000673.1:g.74168512G>T	GRCh37
NC_000011.8:g.73846160G>T	NCBI36
NG_011833.1:g.15089C>A , LRG_439:g.15089C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000310128.9:c.97C>A MANE Select	ENSP00000310557.4:p.Pro33Thr
ENST00000310128.8:c.97C>A	ENSP00000310557.4:p.Pro33Thr
ENST00000525550.1:c.97C>A	ENSP00000433633.1:p.Pro33Thr
ENST00000529425.5:c.97C>A	ENSP00000434890.1:p.Pro33Thr
ENST00000531854.5:c.97C>A	ENSP00000433697.1:p.Pro33Thr
ENST00000532569.5:c.97C>A	ENSP00000431739.1:p.Pro33Thr
NM_005472.4:c.97C>A , LRG_439t1:c.97C>A	NP_005463.1:p.Pro33Thr
XM_011544713.1:c.229C>A	XP_011543015.1:p.Pro77Thr
XM_011544713.2:c.229C>A	XP_011543015.1:p.Pro77Thr
XM_017017047.1:c.97C>A	XP_016872536.1:p.Pro33Thr
XM_017017048.1:c.97C>A	XP_016872537.1:p.Pro33Thr
XM_017017049.1:c.97C>A	XP_016872538.1:p.Pro33Thr
XM_017017051.2:c.97C>A	XP_016872540.1:p.Pro33Thr
XM_017017052.1:c.97C>A	XP_016872541.1:p.Pro33Thr
NM_005472.5:c.97C>A MANE Select	NP_005463.1:p.Pro33Thr