Canonical Allele Identifier: CA381974273

Gene: KCNE3

Linked Data

• gnomAD v4: 11-74457563-T-C
• MyVariant Identifiers: chr11:g.74168608T>C (hg19) ; chr11:g.74457563T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457563T>C , CM000673.2:g.74457563T>C	GRCh38
NC_000011.9:g.74168608T>C , CM000673.1:g.74168608T>C	GRCh37
NC_000011.8:g.73846256T>C	NCBI36
NG_011833.1:g.14993A>G , LRG_439:g.14993A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310128.9:c.1A>G MANE Select	ENSP00000310557.4:p.Met1Val
ENST00000310128.8:c.1A>G	ENSP00000310557.4:p.Met1Val
ENST00000525550.1:c.1A>G	ENSP00000433633.1:p.Met1Val
ENST00000526855.1:c.1A>G	ENSP00000435539.1:p.Met1Val
ENST00000529425.5:c.1A>G	ENSP00000434890.1:p.Met1Val
ENST00000531854.5:c.1A>G	ENSP00000433697.1:p.Met1Val
ENST00000532569.5:c.1A>G	ENSP00000431739.1:p.Met1Val
NM_005472.4:c.1A>G , LRG_439t1:c.1A>G	NP_005463.1:p.Met1Val
XM_011544713.1:c.133A>G	XP_011543015.1:p.Met45Val
XM_011544713.2:c.133A>G	XP_011543015.1:p.Met45Val
XM_017017047.1:c.1A>G	XP_016872536.1:p.Met1Val
XM_017017048.1:c.1A>G	XP_016872537.1:p.Met1Val
XM_017017049.1:c.1A>G	XP_016872538.1:p.Met1Val
XM_017017051.2:c.1A>G	XP_016872540.1:p.Met1Val
XM_017017052.1:c.1A>G	XP_016872541.1:p.Met1Val
NM_005472.5:c.1A>G MANE Select	NP_005463.1:p.Met1Val