Canonical Allele Identifier: CA694289817

Gene: NALCN

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101407725C>G , CM000675.2:g.101407725C>G	GRCh38
NC_000013.10:g.102060076C>G , CM000675.1:g.102060076C>G	GRCh37
NC_000013.9:g.100858077C>G	NCBI36
NG_053176.1:g.14482G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.-39-8560G>C MANE Select	ENSP00000251127.6:n.-39-8560G>C
ENST00000648359.1:c.-39-8560G>C	ENSP00000497465.1:n.-39-8560G>C
ENST00000674840.1:n.60-8560G>C
ENST00000674904.1:n.126-8560G>C
ENST00000675150.1:c.-39-8560G>C	ENSP00000502680.1:n.-39-8560G>C
ENST00000675332.1:c.-39-8560G>C	ENSP00000501955.1:n.-39-8560G>C
ENST00000675415.1:n.145-8560G>C
ENST00000675802.1:c.-39-8560G>C	ENSP00000501818.1:n.-39-8560G>C
ENST00000676315.1:c.-39-8560G>C	ENSP00000501603.1:n.-39-8560G>C
ENST00000676357.1:n.182-8560G>C
ENST00000676439.1:n.136-8560G>C
ENST00000251127.10:c.-39-8560G>C	ENSP00000251127.6:n.-39-8560G>C
ENST00000470333.1:n.58-8560G>C
ENST00000497170.5:n.151-8560G>C
NM_052867.2:c.-39-8560G>C	NP_443099.1:n.-39-8560G>C
XM_011521067.1:c.19-8560G>C	XP_011519369.1:n.19-8560G>C
XM_011521068.1:c.-39-8560G>C	XP_011519370.1:n.-39-8560G>C
XM_011521069.1:c.19-8560G>C	XP_011519371.1:n.19-8560G>C
XM_011521070.1:c.19-8560G>C	XP_011519372.1:n.19-8560G>C
NM_001350748.1:c.-39-8560G>C	NP_001337677.1:n.-39-8560G>C
NM_001350749.1:c.-39-8560G>C	NP_001337678.1:n.-39-8560G>C
NM_001350750.1:c.-39-8560G>C	NP_001337679.1:n.-39-8560G>C
NM_001350751.1:c.-39-8560G>C	NP_001337680.1:n.-39-8560G>C
NM_052867.3:c.-39-8560G>C	NP_443099.1:n.-39-8560G>C
XM_011521067.2:c.19-8560G>C	XP_011519369.1:n.19-8560G>C
XM_011521069.2:c.19-8560G>C	XP_011519371.1:n.19-8560G>C
XM_024449336.1:c.19-8560G>C	XP_024305104.1:n.19-8560G>C
NM_052867.4:c.-39-8560G>C MANE Select	NP_443099.1:n.-39-8560G>C
NM_001350748.2:c.-39-8560G>C	NP_001337677.1:n.-39-8560G>C
NM_001350749.2:c.-39-8560G>C	NP_001337678.1:n.-39-8560G>C
NM_001350750.2:c.-39-8560G>C	NP_001337679.1:n.-39-8560G>C
NM_001350751.2:c.-39-8560G>C	NP_001337680.1:n.-39-8560G>C