Canonical Allele Identifier: CA388650261

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733922T>G (hg19) ; chr13:g.101081571T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081571T>G , CM000675.2:g.101081571T>G	GRCh38
NC_000013.10:g.101733922T>G , CM000675.1:g.101733922T>G	GRCh37
NC_000013.9:g.100531923T>G	NCBI36
NG_053176.1:g.340636A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3841A>C MANE Select	ENSP00000251127.6:p.Thr1281Pro
ENST00000648359.1:c.3841A>C	ENSP00000497465.1:p.Thr1281Pro
ENST00000675150.1:c.3562A>C	ENSP00000502680.1:p.Thr1188Pro
ENST00000675332.1:c.3928A>C	ENSP00000501955.1:p.Thr1310Pro
ENST00000676315.1:c.3754A>C	ENSP00000501603.1:p.Thr1252Pro
ENST00000251127.10:c.3841A>C	ENSP00000251127.6:p.Thr1281Pro
NM_052867.2:c.3841A>C	NP_443099.1:p.Thr1281Pro
XM_011521067.1:c.3898A>C	XP_011519369.1:p.Thr1300Pro
XM_011521068.1:c.3841A>C	XP_011519370.1:p.Thr1281Pro
XM_011521069.1:c.3811A>C	XP_011519371.1:p.Thr1271Pro
XM_011521070.1:c.3619A>C	XP_011519372.1:p.Thr1207Pro
NM_001350748.1:c.3928A>C	NP_001337677.1:p.Thr1310Pro
NM_001350749.1:c.3841A>C	NP_001337678.1:p.Thr1281Pro
NM_001350750.1:c.3754A>C	NP_001337679.1:p.Thr1252Pro
NM_001350751.1:c.3754A>C	NP_001337680.1:p.Thr1252Pro
NM_052867.3:c.3841A>C	NP_443099.1:p.Thr1281Pro
XM_011521067.2:c.3898A>C	XP_011519369.1:p.Thr1300Pro
XM_011521069.2:c.3811A>C	XP_011519371.1:p.Thr1271Pro
XM_017020536.2:c.3394A>C	XP_016876025.1:p.Thr1132Pro
XM_017020537.1:c.3076A>C	XP_016876026.1:p.Thr1026Pro
XM_024449336.1:c.3985A>C	XP_024305104.1:p.Thr1329Pro
NM_052867.4:c.3841A>C MANE Select	NP_443099.1:p.Thr1281Pro
NM_001350748.2:c.3928A>C	NP_001337677.1:p.Thr1310Pro
NM_001350749.2:c.3841A>C	NP_001337678.1:p.Thr1281Pro
NM_001350750.2:c.3754A>C	NP_001337679.1:p.Thr1252Pro
NM_001350751.2:c.3754A>C	NP_001337680.1:p.Thr1252Pro