Canonical Allele Identifier: CA388650452

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733980T>C (hg19) ; chr13:g.101081629T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081629T>C , CM000675.2:g.101081629T>C	GRCh38
NC_000013.10:g.101733980T>C , CM000675.1:g.101733980T>C	GRCh37
NC_000013.9:g.100531981T>C	NCBI36
NG_053176.1:g.340578A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3783A>G MANE Select	ENSP00000251127.6:p.Ile1261Met
ENST00000648359.1:c.3783A>G	ENSP00000497465.1:p.Ile1261Met
ENST00000675150.1:c.3504A>G	ENSP00000502680.1:p.Ile1168Met
ENST00000675332.1:c.3870A>G	ENSP00000501955.1:p.Ile1290Met
ENST00000676315.1:c.3696A>G	ENSP00000501603.1:p.Ile1232Met
ENST00000251127.10:c.3783A>G	ENSP00000251127.6:p.Ile1261Met
NM_052867.2:c.3783A>G	NP_443099.1:p.Ile1261Met
XM_011521067.1:c.3840A>G	XP_011519369.1:p.Ile1280Met
XM_011521068.1:c.3783A>G	XP_011519370.1:p.Ile1261Met
XM_011521069.1:c.3753A>G	XP_011519371.1:p.Ile1251Met
XM_011521070.1:c.3561A>G	XP_011519372.1:p.Ile1187Met
NM_001350748.1:c.3870A>G	NP_001337677.1:p.Ile1290Met
NM_001350749.1:c.3783A>G	NP_001337678.1:p.Ile1261Met
NM_001350750.1:c.3696A>G	NP_001337679.1:p.Ile1232Met
NM_001350751.1:c.3696A>G	NP_001337680.1:p.Ile1232Met
NM_052867.3:c.3783A>G	NP_443099.1:p.Ile1261Met
XM_011521067.2:c.3840A>G	XP_011519369.1:p.Ile1280Met
XM_011521069.2:c.3753A>G	XP_011519371.1:p.Ile1251Met
XM_017020536.2:c.3336A>G	XP_016876025.1:p.Ile1112Met
XM_017020537.1:c.3018A>G	XP_016876026.1:p.Ile1006Met
XM_024449336.1:c.3927A>G	XP_024305104.1:p.Ile1309Met
NM_052867.4:c.3783A>G MANE Select	NP_443099.1:p.Ile1261Met
NM_001350748.2:c.3870A>G	NP_001337677.1:p.Ile1290Met
NM_001350749.2:c.3783A>G	NP_001337678.1:p.Ile1261Met
NM_001350750.2:c.3696A>G	NP_001337679.1:p.Ile1232Met
NM_001350751.2:c.3696A>G	NP_001337680.1:p.Ile1232Met