Canonical Allele Identifier: CA7035672

Gene: NALCN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101107503G>A , CM000675.2:g.101107503G>A	GRCh38
NC_000013.10:g.101759854G>A , CM000675.1:g.101759854G>A	GRCh37
NC_000013.9:g.100557855G>A	NCBI36
NG_053176.1:g.314704C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.2563C>T MANE Select	ENSP00000251127.6:p.Arg855Ter
ENST00000648359.1:c.2563C>T	ENSP00000497465.1:p.Arg855Ter
ENST00000675150.1:c.2284C>T	ENSP00000502680.1:p.Arg762Ter
ENST00000675332.1:c.2650C>T	ENSP00000501955.1:p.Arg884Ter
ENST00000676315.1:c.2476C>T	ENSP00000501603.1:p.Arg826Ter
ENST00000251127.10:c.2563C>T	ENSP00000251127.6:p.Arg855Ter
NM_052867.2:c.2563C>T	NP_443099.1:p.Arg855Ter
XM_011521067.1:c.2620C>T	XP_011519369.1:p.Arg874Ter
XM_011521068.1:c.2563C>T	XP_011519370.1:p.Arg855Ter
XM_011521069.1:c.2533C>T	XP_011519371.1:p.Arg845Ter
XM_011521070.1:c.2341C>T	XP_011519372.1:p.Arg781Ter
NM_001350748.1:c.2650C>T	NP_001337677.1:p.Arg884Ter
NM_001350749.1:c.2563C>T	NP_001337678.1:p.Arg855Ter
NM_001350750.1:c.2476C>T	NP_001337679.1:p.Arg826Ter
NM_001350751.1:c.2476C>T	NP_001337680.1:p.Arg826Ter
NM_052867.3:c.2563C>T	NP_443099.1:p.Arg855Ter
XM_011521067.2:c.2620C>T	XP_011519369.1:p.Arg874Ter
XM_011521069.2:c.2533C>T	XP_011519371.1:p.Arg845Ter
XM_017020536.2:c.2116C>T	XP_016876025.1:p.Arg706Ter
XM_017020537.1:c.1798C>T	XP_016876026.1:p.Arg600Ter
XM_024449336.1:c.2707C>T	XP_024305104.1:p.Arg903Ter
NM_052867.4:c.2563C>T MANE Select	NP_443099.1:p.Arg855Ter
NM_001350748.2:c.2650C>T	NP_001337677.1:p.Arg884Ter
NM_001350749.2:c.2563C>T	NP_001337678.1:p.Arg855Ter
NM_001350750.2:c.2476C>T	NP_001337679.1:p.Arg826Ter
NM_001350751.2:c.2476C>T	NP_001337680.1:p.Arg826Ter