Canonical Allele Identifier: CA2114388853

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081584_101081586delinsGTA , CM000675.2:g.101081584_101081586delinsGTA	GRCh38
NC_000013.10:g.101733935_101733937delinsGTA , CM000675.1:g.101733935_101733937delinsGTA	GRCh37
NC_000013.9:g.100531936_100531938delinsGTA	NCBI36
NG_053176.1:g.340621_340623delinsTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3826_3828delinsTAC MANE Select	ENSP00000251127.6:p.Tyr1276=
ENST00000648359.1:c.3826_3828delinsTAC	ENSP00000497465.1:p.Tyr1276=
ENST00000675150.1:c.3547_3549delinsTAC	ENSP00000502680.1:p.Tyr1183=
ENST00000675332.1:c.3913_3915delinsTAC	ENSP00000501955.1:p.Tyr1305=
ENST00000676315.1:c.3739_3741delinsTAC	ENSP00000501603.1:p.Tyr1247=
ENST00000251127.10:c.3826_3828delinsTAC	ENSP00000251127.6:p.Tyr1276=
NM_052867.2:c.3826_3828delinsTAC	NP_443099.1:p.Tyr1276=
XM_011521067.1:c.3883_3885delinsTAC	XP_011519369.1:p.Tyr1295=
XM_011521068.1:c.3826_3828delinsTAC	XP_011519370.1:p.Tyr1276=
XM_011521069.1:c.3796_3798delinsTAC	XP_011519371.1:p.Tyr1266=
XM_011521070.1:c.3604_3606delinsTAC	XP_011519372.1:p.Tyr1202=
NM_001350748.1:c.3913_3915delinsTAC	NP_001337677.1:p.Tyr1305=
NM_001350749.1:c.3826_3828delinsTAC	NP_001337678.1:p.Tyr1276=
NM_001350750.1:c.3739_3741delinsTAC	NP_001337679.1:p.Tyr1247=
NM_001350751.1:c.3739_3741delinsTAC	NP_001337680.1:p.Tyr1247=
NM_052867.3:c.3826_3828delinsTAC	NP_443099.1:p.Tyr1276=
XM_011521067.2:c.3883_3885delinsTAC	XP_011519369.1:p.Tyr1295=
XM_011521069.2:c.3796_3798delinsTAC	XP_011519371.1:p.Tyr1266=
XM_017020536.2:c.3379_3381delinsTAC	XP_016876025.1:p.Tyr1127=
XM_017020537.1:c.3061_3063delinsTAC	XP_016876026.1:p.Tyr1021=
XM_024449336.1:c.3970_3972delinsTAC	XP_024305104.1:p.Tyr1324=
NM_052867.4:c.3826_3828delinsTAC MANE Select	NP_443099.1:p.Tyr1276=
NM_001350748.2:c.3913_3915delinsTAC	NP_001337677.1:p.Tyr1305=
NM_001350749.2:c.3826_3828delinsTAC	NP_001337678.1:p.Tyr1276=
NM_001350750.2:c.3739_3741delinsTAC	NP_001337679.1:p.Tyr1247=
NM_001350751.2:c.3739_3741delinsTAC	NP_001337680.1:p.Tyr1247=