Canonical Allele Identifier: CA388671564

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101795553A>C (hg19) ; chr13:g.101143202A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101143202A>C , CM000675.2:g.101143202A>C	GRCh38
NC_000013.10:g.101795553A>C , CM000675.1:g.101795553A>C	GRCh37
NC_000013.9:g.100593554A>C	NCBI36
NG_053176.1:g.279005T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1996T>G MANE Select	ENSP00000251127.6:p.Phe666Val
ENST00000467264.2:c.188T>G
ENST00000648359.1:c.1996T>G	ENSP00000497465.1:p.Phe666Val
ENST00000675150.1:c.1840-18521T>G	ENSP00000502680.1:n.1840-18521T>G
ENST00000675332.1:c.1996T>G	ENSP00000501955.1:p.Phe666Val
ENST00000675802.1:c.1996T>G	ENSP00000501818.1:p.Phe666Val
ENST00000676315.1:c.1909T>G	ENSP00000501603.1:p.Phe637Val
ENST00000251127.10:c.1996T>G	ENSP00000251127.6:p.Phe666Val
ENST00000467264.1:n.20T>G
ENST00000497170.5:n.2150T>G
NM_052867.2:c.1996T>G	NP_443099.1:p.Phe666Val
XM_011521067.1:c.2053T>G	XP_011519369.1:p.Phe685Val
XM_011521068.1:c.1996T>G	XP_011519370.1:p.Phe666Val
XM_011521069.1:c.1966T>G	XP_011519371.1:p.Phe656Val
XM_011521070.1:c.1897-18521T>G	XP_011519372.1:n.1897-18521T>G
NM_001350748.1:c.1996T>G	NP_001337677.1:p.Phe666Val
NM_001350749.1:c.1996T>G	NP_001337678.1:p.Phe666Val
NM_001350750.1:c.1909T>G	NP_001337679.1:p.Phe637Val
NM_001350751.1:c.1909T>G	NP_001337680.1:p.Phe637Val
NM_052867.3:c.1996T>G	NP_443099.1:p.Phe666Val
XM_011521067.2:c.2053T>G	XP_011519369.1:p.Phe685Val
XM_011521069.2:c.1966T>G	XP_011519371.1:p.Phe656Val
XM_017020536.2:c.1549T>G	XP_016876025.1:p.Phe517Val
XM_017020537.1:c.1231T>G	XP_016876026.1:p.Phe411Val
XM_024449336.1:c.2053T>G	XP_024305104.1:p.Phe685Val
NM_052867.4:c.1996T>G MANE Select	NP_443099.1:p.Phe666Val
NM_001350748.2:c.1996T>G	NP_001337677.1:p.Phe666Val
NM_001350749.2:c.1996T>G	NP_001337678.1:p.Phe666Val
NM_001350750.2:c.1909T>G	NP_001337679.1:p.Phe637Val
NM_001350751.2:c.1909T>G	NP_001337680.1:p.Phe637Val