Canonical Allele Identifier: CA6184882

Gene: KCNE3

Linked Data

• dbSNP Id: rs377606406
• ExAC: 11:74168619 A / G
• gnomAD v2: 11-74168619-A-G
• gnomAD v3: 11-74457574-A-G
• gnomAD v4: 11-74457574-A-G
• MyVariant Identifiers: chr11:g.74168619A>G (hg19) ; chr11:g.74457574A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457574A>G , CM000673.2:g.74457574A>G	GRCh38
NC_000011.9:g.74168619A>G , CM000673.1:g.74168619A>G	GRCh37
NC_000011.8:g.73846267A>G	NCBI36
NG_011833.1:g.14982T>C , LRG_439:g.14982T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310128.9:c.-11T>C MANE Select	ENSP00000310557.4:n.-11T>C
ENST00000310128.8:c.-11T>C	ENSP00000310557.4:n.-11T>C
ENST00000525550.1:c.-11T>C	ENSP00000433633.1:n.-11T>C
ENST00000526855.1:c.-11T>C	ENSP00000435539.1:n.-11T>C
ENST00000529425.5:c.-11T>C	ENSP00000434890.1:n.-11T>C
ENST00000531854.5:c.-11T>C	ENSP00000433697.1:n.-11T>C
ENST00000532569.5:c.-11T>C	ENSP00000431739.1:n.-11T>C
NM_005472.4:c.-11T>C , LRG_439t1:c.-11T>C	NP_005463.1:n.-11T>C
XM_011544713.1:c.122T>C	XP_011543015.1:p.Ile41Thr
XM_011544713.2:c.122T>C	XP_011543015.1:p.Ile41Thr
XM_017017047.1:c.-11T>C	XP_016872536.1:n.-11T>C
XM_017017048.1:c.-11T>C	XP_016872537.1:n.-11T>C
XM_017017049.1:c.-11T>C	XP_016872538.1:n.-11T>C
XM_017017051.2:c.-11T>C	XP_016872540.1:n.-11T>C
XM_017017052.1:c.-11T>C	XP_016872541.1:n.-11T>C
NM_005472.5:c.-11T>C MANE Select	NP_005463.1:n.-11T>C