Canonical Allele Identifier: CA2615094089

Gene: KCNE3

Linked Data

• gnomAD v4: 11-74457188-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457188G>T , CM000673.2:g.74457188G>T	GRCh38
NC_000011.9:g.74168233G>T , CM000673.1:g.74168233G>T	GRCh37
NC_000011.8:g.73845881G>T	NCBI36
NG_011833.1:g.15368C>A , LRG_439:g.15368C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310128.9:c.*64C>A MANE Select	ENSP00000310557.4:n.*64C>A
ENST00000310128.8:c.*64C>A	ENSP00000310557.4:n.*64C>A
ENST00000525550.1:c.*64C>A	ENSP00000433633.1:n.*64C>A
NM_005472.4:c.*64C>A , LRG_439t1:c.*64C>A	NP_005463.1:n.*64C>A
XM_011544713.1:c.*64C>A	XP_011543015.1:n.*64C>A
XM_011544713.2:c.*64C>A	XP_011543015.1:n.*64C>A
XM_017017047.1:c.*64C>A	XP_016872536.1:n.*64C>A
XM_017017048.1:c.*64C>A	XP_016872537.1:n.*64C>A
XM_017017049.1:c.*64C>A	XP_016872538.1:n.*64C>A
XM_017017051.2:c.*64C>A	XP_016872540.1:n.*64C>A
XM_017017052.1:c.*64C>A	XP_016872541.1:n.*64C>A
NM_005472.5:c.*64C>A MANE Select	NP_005463.1:n.*64C>A