Canonical Allele Identifier: CA484550609

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101073674A>G , CM000675.2:g.101073674A>G	GRCh38
NC_000013.10:g.101726026A>G , CM000675.1:g.101726026A>G	GRCh37
NC_000013.9:g.100524027A>G	NCBI36
NG_053176.1:g.348533T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.4107T>C MANE Select	ENSP00000251127.6:p.His1369=
ENST00000648359.1:c.4107T>C	ENSP00000497465.1:p.His1369=
ENST00000675150.1:c.3828T>C	ENSP00000502680.1:p.His1276=
ENST00000675332.1:c.4194T>C	ENSP00000501955.1:p.His1398=
ENST00000676315.1:c.4020T>C	ENSP00000501603.1:p.His1340=
ENST00000251127.10:c.4107T>C	ENSP00000251127.6:p.His1369=
NM_052867.2:c.4107T>C	NP_443099.1:p.His1369=
XM_011521067.1:c.4164T>C	XP_011519369.1:p.His1388=
XM_011521068.1:c.4107T>C	XP_011519370.1:p.His1369=
XM_011521069.1:c.4077T>C	XP_011519371.1:p.His1359=
XM_011521070.1:c.3885T>C	XP_011519372.1:p.His1295=
NM_001350748.1:c.4194T>C	NP_001337677.1:p.His1398=
NM_001350749.1:c.4107T>C	NP_001337678.1:p.His1369=
NM_001350750.1:c.4020T>C	NP_001337679.1:p.His1340=
NM_001350751.1:c.4020T>C	NP_001337680.1:p.His1340=
NM_052867.3:c.4107T>C	NP_443099.1:p.His1369=
XM_011521067.2:c.4164T>C	XP_011519369.1:p.His1388=
XM_011521069.2:c.4077T>C	XP_011519371.1:p.His1359=
XM_017020536.2:c.3660T>C	XP_016876025.1:p.His1220=
XM_017020537.1:c.3342T>C	XP_016876026.1:p.His1114=
XM_024449336.1:c.4251T>C	XP_024305104.1:p.His1417=
NM_052867.4:c.4107T>C MANE Select	NP_443099.1:p.His1369=
NM_001350748.2:c.4194T>C	NP_001337677.1:p.His1398=
NM_001350749.2:c.4107T>C	NP_001337678.1:p.His1369=
NM_001350750.2:c.4020T>C	NP_001337679.1:p.His1340=
NM_001350751.2:c.4020T>C	NP_001337680.1:p.His1340=