Canonical Allele Identifier: CA388653333

Gene: NALCN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101095574C>T , CM000675.2:g.101095574C>T	GRCh38
NC_000013.10:g.101747925C>T , CM000675.1:g.101747925C>T	GRCh37
NC_000013.9:g.100545926C>T	NCBI36
NG_053176.1:g.326633G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3269G>A MANE Select	ENSP00000251127.6:p.Trp1090Ter
ENST00000648359.1:c.3269G>A	ENSP00000497465.1:p.Trp1090Ter
ENST00000675150.1:c.2990G>A	ENSP00000502680.1:p.Trp997Ter
ENST00000675332.1:c.3356G>A	ENSP00000501955.1:p.Trp1119Ter
ENST00000676315.1:c.3182G>A	ENSP00000501603.1:p.Trp1061Ter
ENST00000251127.10:c.3269G>A	ENSP00000251127.6:p.Trp1090Ter
NM_052867.2:c.3269G>A	NP_443099.1:p.Trp1090Ter
XM_011521067.1:c.3326G>A	XP_011519369.1:p.Trp1109Ter
XM_011521068.1:c.3269G>A	XP_011519370.1:p.Trp1090Ter
XM_011521069.1:c.3239G>A	XP_011519371.1:p.Trp1080Ter
XM_011521070.1:c.3047G>A	XP_011519372.1:p.Trp1016Ter
NM_001350748.1:c.3356G>A	NP_001337677.1:p.Trp1119Ter
NM_001350749.1:c.3269G>A	NP_001337678.1:p.Trp1090Ter
NM_001350750.1:c.3182G>A	NP_001337679.1:p.Trp1061Ter
NM_001350751.1:c.3182G>A	NP_001337680.1:p.Trp1061Ter
NM_052867.3:c.3269G>A	NP_443099.1:p.Trp1090Ter
XM_011521067.2:c.3326G>A	XP_011519369.1:p.Trp1109Ter
XM_011521069.2:c.3239G>A	XP_011519371.1:p.Trp1080Ter
XM_017020536.2:c.2822G>A	XP_016876025.1:p.Trp941Ter
XM_017020537.1:c.2504G>A	XP_016876026.1:p.Trp835Ter
XM_024449336.1:c.3413G>A	XP_024305104.1:p.Trp1138Ter
NM_052867.4:c.3269G>A MANE Select	NP_443099.1:p.Trp1090Ter
NM_001350748.2:c.3356G>A	NP_001337677.1:p.Trp1119Ter
NM_001350749.2:c.3269G>A	NP_001337678.1:p.Trp1090Ter
NM_001350750.2:c.3182G>A	NP_001337679.1:p.Trp1061Ter
NM_001350751.2:c.3182G>A	NP_001337680.1:p.Trp1061Ter