Canonical Allele Identifier: CA2114388852

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081584G= , CM000675.2:g.101081584G=	GRCh38
NC_000013.10:g.101733935G= , CM000675.1:g.101733935G=	GRCh37
NC_000013.9:g.100531936G=	NCBI36
NG_053176.1:g.340623C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3828C= MANE Select	ENSP00000251127.6:p.Tyr1276=
ENST00000648359.1:c.3828C=	ENSP00000497465.1:p.Tyr1276=
ENST00000675150.1:c.3549C=	ENSP00000502680.1:p.Tyr1183=
ENST00000675332.1:c.3915C=	ENSP00000501955.1:p.Tyr1305=
ENST00000676315.1:c.3741C=	ENSP00000501603.1:p.Tyr1247=
ENST00000251127.10:c.3828C=	ENSP00000251127.6:p.Tyr1276=
NM_052867.2:c.3828C=	NP_443099.1:p.Tyr1276=
XM_011521067.1:c.3885C=	XP_011519369.1:p.Tyr1295=
XM_011521068.1:c.3828C=	XP_011519370.1:p.Tyr1276=
XM_011521069.1:c.3798C=	XP_011519371.1:p.Tyr1266=
XM_011521070.1:c.3606C=	XP_011519372.1:p.Tyr1202=
NM_001350748.1:c.3915C=	NP_001337677.1:p.Tyr1305=
NM_001350749.1:c.3828C=	NP_001337678.1:p.Tyr1276=
NM_001350750.1:c.3741C=	NP_001337679.1:p.Tyr1247=
NM_001350751.1:c.3741C=	NP_001337680.1:p.Tyr1247=
NM_052867.3:c.3828C=	NP_443099.1:p.Tyr1276=
XM_011521067.2:c.3885C=	XP_011519369.1:p.Tyr1295=
XM_011521069.2:c.3798C=	XP_011519371.1:p.Tyr1266=
XM_017020536.2:c.3381C=	XP_016876025.1:p.Tyr1127=
XM_017020537.1:c.3063C=	XP_016876026.1:p.Tyr1021=
XM_024449336.1:c.3972C=	XP_024305104.1:p.Tyr1324=
NM_052867.4:c.3828C= MANE Select	NP_443099.1:p.Tyr1276=
NM_001350748.2:c.3915C=	NP_001337677.1:p.Tyr1305=
NM_001350749.2:c.3828C=	NP_001337678.1:p.Tyr1276=
NM_001350750.2:c.3741C=	NP_001337679.1:p.Tyr1247=
NM_001350751.2:c.3741C=	NP_001337680.1:p.Tyr1247=