Canonical Allele Identifier: CA381973911

Gene: KCNE3

Linked Data

• MyVariant Identifiers: chr11:g.74168432C>G (hg19) ; chr11:g.74457387C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457387C>G , CM000673.2:g.74457387C>G	GRCh38
NC_000011.9:g.74168432C>G , CM000673.1:g.74168432C>G	GRCh37
NC_000011.8:g.73846080C>G	NCBI36
NG_011833.1:g.15169G>C , LRG_439:g.15169G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310128.9:c.177G>C MANE Select	ENSP00000310557.4:p.Met59Ile
ENST00000310128.8:c.177G>C	ENSP00000310557.4:p.Met59Ile
ENST00000525550.1:c.177G>C	ENSP00000433633.1:p.Met59Ile
ENST00000532569.5:c.177G>C	ENSP00000431739.1:p.Met59Ile
NM_005472.4:c.177G>C , LRG_439t1:c.177G>C	NP_005463.1:p.Met59Ile
XM_011544713.1:c.309G>C	XP_011543015.1:p.Met103Ile
XM_011544713.2:c.309G>C	XP_011543015.1:p.Met103Ile
XM_017017047.1:c.177G>C	XP_016872536.1:p.Met59Ile
XM_017017048.1:c.177G>C	XP_016872537.1:p.Met59Ile
XM_017017049.1:c.177G>C	XP_016872538.1:p.Met59Ile
XM_017017051.2:c.177G>C	XP_016872540.1:p.Met59Ile
XM_017017052.1:c.177G>C	XP_016872541.1:p.Met59Ile
NM_005472.5:c.177G>C MANE Select	NP_005463.1:p.Met59Ile