Canonical Allele Identifier: CA1982893237

Gene: KCNE3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.74457268_74457269delinsCG , CM000673.2:g.74457268_74457269delinsCG	GRCh38
NC_000011.9:g.74168313_74168314delinsCG , CM000673.1:g.74168313_74168314delinsCG	GRCh37
NC_000011.8:g.73845961_73845962delinsCG	NCBI36
NG_011833.1:g.15287_15288delinsCG , LRG_439:g.15287_15288delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000310128.9:c.295_296delinsCG MANE Select	ENSP00000310557.4:p.Arg99=
ENST00000310128.8:c.295_296delinsCG	ENSP00000310557.4:p.Arg99=
ENST00000525550.1:c.295_296delinsCG	ENSP00000433633.1:p.Arg99=
ENST00000532569.5:c.295_296delinsCG	ENSP00000431739.1:p.Arg99=
NM_005472.4:c.295_296delinsCG , LRG_439t1:c.295_296delinsCG	NP_005463.1:p.Arg99=
XM_011544713.1:c.427_428delinsCG	XP_011543015.1:p.Arg143=
XM_011544713.2:c.427_428delinsCG	XP_011543015.1:p.Arg143=
XM_017017047.1:c.295_296delinsCG	XP_016872536.1:p.Arg99=
XM_017017048.1:c.295_296delinsCG	XP_016872537.1:p.Arg99=
XM_017017049.1:c.295_296delinsCG	XP_016872538.1:p.Arg99=
XM_017017051.2:c.295_296delinsCG	XP_016872540.1:p.Arg99=
XM_017017052.1:c.295_296delinsCG	XP_016872541.1:p.Arg99=
NM_005472.5:c.295_296delinsCG MANE Select	NP_005463.1:p.Arg99=