Canonical Allele Identifier: CA475842786

Gene: KCNE3

Linked Data

• gnomAD v4: 11-74457321-G-C
• MyVariant Identifiers: chr11:g.74168366G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457321G>C , CM000673.2:g.74457321G>C	GRCh38
NC_000011.9:g.74168366G>C , CM000673.1:g.74168366G>C	GRCh37
NC_000011.8:g.73846014G>C	NCBI36
NG_011833.1:g.15235C>G , LRG_439:g.15235C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310128.9:c.243C>G MANE Select	ENSP00000310557.4:p.Arg81=
ENST00000310128.8:c.243C>G	ENSP00000310557.4:p.Arg81=
ENST00000525550.1:c.243C>G	ENSP00000433633.1:p.Arg81=
ENST00000532569.5:c.243C>G	ENSP00000431739.1:p.Arg81=
NM_005472.4:c.243C>G , LRG_439t1:c.243C>G	NP_005463.1:p.Arg81=
XM_011544713.1:c.375C>G	XP_011543015.1:p.Arg125=
XM_011544713.2:c.375C>G	XP_011543015.1:p.Arg125=
XM_017017047.1:c.243C>G	XP_016872536.1:p.Arg81=
XM_017017048.1:c.243C>G	XP_016872537.1:p.Arg81=
XM_017017049.1:c.243C>G	XP_016872538.1:p.Arg81=
XM_017017051.2:c.243C>G	XP_016872540.1:p.Arg81=
XM_017017052.1:c.243C>G	XP_016872541.1:p.Arg81=
NM_005472.5:c.243C>G MANE Select	NP_005463.1:p.Arg81=