Canonical Allele Identifier: CA10639415

Gene: KCNE3

Linked Data

• ClinVar Variation Id: 1270048
• ClinVar RCV Id: RCV001684206
• dbSNP Id: rs11236111
• gnomAD v2: 11-74168217-T-C
• gnomAD v3: 11-74457172-T-C
• gnomAD v4: 11-74457172-T-C
• MyVariant Identifiers: chr11:g.74168217T>C (hg19) ; chr11:g.74457172T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457172T>C , CM000673.2:g.74457172T>C	GRCh38
NC_000011.9:g.74168217T>C , CM000673.1:g.74168217T>C	GRCh37
NC_000011.8:g.73845865T>C	NCBI36
NG_011833.1:g.15384A>G , LRG_439:g.15384A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000310128.9:c.*80A>G MANE Select	ENSP00000310557.4:n.*80A>G
ENST00000310128.8:c.*80A>G	ENSP00000310557.4:n.*80A>G
ENST00000525550.1:c.*80A>G	ENSP00000433633.1:n.*80A>G
NM_005472.4:c.*80A>G , LRG_439t1:c.*80A>G	NP_005463.1:n.*80A>G
XM_011544713.1:c.*80A>G	XP_011543015.1:n.*80A>G
XM_011544713.2:c.*80A>G	XP_011543015.1:n.*80A>G
XM_017017047.1:c.*80A>G	XP_016872536.1:n.*80A>G
XM_017017048.1:c.*80A>G	XP_016872537.1:n.*80A>G
XM_017017049.1:c.*80A>G	XP_016872538.1:n.*80A>G
XM_017017051.2:c.*80A>G	XP_016872540.1:n.*80A>G
XM_017017052.1:c.*80A>G	XP_016872541.1:n.*80A>G
NM_005472.5:c.*80A>G MANE Select	NP_005463.1:n.*80A>G