Canonical Allele Identifier: CA381973676

Gene: KCNE3

Linked Data

• MyVariant Identifiers: chr11:g.74168321G>C (hg19) ; chr11:g.74457276G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457276G>C , CM000673.2:g.74457276G>C	GRCh38
NC_000011.9:g.74168321G>C , CM000673.1:g.74168321G>C	GRCh37
NC_000011.8:g.73845969G>C	NCBI36
NG_011833.1:g.15280C>G , LRG_439:g.15280C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310128.9:c.288C>G MANE Select	ENSP00000310557.4:p.Ile96Met
ENST00000310128.8:c.288C>G	ENSP00000310557.4:p.Ile96Met
ENST00000525550.1:c.288C>G	ENSP00000433633.1:p.Ile96Met
ENST00000532569.5:c.288C>G	ENSP00000431739.1:p.Ile96Met
NM_005472.4:c.288C>G , LRG_439t1:c.288C>G	NP_005463.1:p.Ile96Met
XM_011544713.1:c.420C>G	XP_011543015.1:p.Ile140Met
XM_011544713.2:c.420C>G	XP_011543015.1:p.Ile140Met
XM_017017047.1:c.288C>G	XP_016872536.1:p.Ile96Met
XM_017017048.1:c.288C>G	XP_016872537.1:p.Ile96Met
XM_017017049.1:c.288C>G	XP_016872538.1:p.Ile96Met
XM_017017051.2:c.288C>G	XP_016872540.1:p.Ile96Met
XM_017017052.1:c.288C>G	XP_016872541.1:p.Ile96Met
NM_005472.5:c.288C>G MANE Select	NP_005463.1:p.Ile96Met