Canonical Allele Identifier: CA475888144

Gene: KCNE3

Linked Data

• MyVariant Identifiers: chr11:g.74168510T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457465T>G , CM000673.2:g.74457465T>G	GRCh38
NC_000011.9:g.74168510T>G , CM000673.1:g.74168510T>G	GRCh37
NC_000011.8:g.73846158T>G	NCBI36
NG_011833.1:g.15091A>C , LRG_439:g.15091A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000310128.9:c.99A>C MANE Select	ENSP00000310557.4:p.Pro33=
ENST00000310128.8:c.99A>C	ENSP00000310557.4:p.Pro33=
ENST00000525550.1:c.99A>C	ENSP00000433633.1:p.Pro33=
ENST00000529425.5:c.99A>C	ENSP00000434890.1:p.Pro33=
ENST00000531854.5:c.99A>C	ENSP00000433697.1:p.Pro33=
ENST00000532569.5:c.99A>C	ENSP00000431739.1:p.Pro33=
NM_005472.4:c.99A>C , LRG_439t1:c.99A>C	NP_005463.1:p.Pro33=
XM_011544713.1:c.231A>C	XP_011543015.1:p.Pro77=
XM_011544713.2:c.231A>C	XP_011543015.1:p.Pro77=
XM_017017047.1:c.99A>C	XP_016872536.1:p.Pro33=
XM_017017048.1:c.99A>C	XP_016872537.1:p.Pro33=
XM_017017049.1:c.99A>C	XP_016872538.1:p.Pro33=
XM_017017051.2:c.99A>C	XP_016872540.1:p.Pro33=
XM_017017052.1:c.99A>C	XP_016872541.1:p.Pro33=
NM_005472.5:c.99A>C MANE Select	NP_005463.1:p.Pro33=