Canonical Allele Identifier: CA388705131

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101944687G>A (hg19) ; chr13:g.101292336G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101292336G>A , CM000675.2:g.101292336G>A	GRCh38
NC_000013.10:g.101944687G>A , CM000675.1:g.101944687G>A	GRCh37
NC_000013.9:g.100742688G>A	NCBI36
NG_053176.1:g.129871C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.830C>T MANE Select	ENSP00000251127.6:p.Ala277Val
ENST00000648359.1:c.830C>T	ENSP00000497465.1:p.Ala277Val
ENST00000674840.1:n.928C>T
ENST00000674904.1:n.910C>T
ENST00000675075.1:n.432C>T
ENST00000675150.1:c.830C>T	ENSP00000502680.1:p.Ala277Val
ENST00000675332.1:c.830C>T	ENSP00000501955.1:p.Ala277Val
ENST00000675415.1:n.1013C>T
ENST00000675594.1:c.*267C>T	ENSP00000502490.1:n.*267C>T
ENST00000675802.1:c.830C>T	ENSP00000501818.1:p.Ala277Val
ENST00000676315.1:c.830C>T	ENSP00000501603.1:p.Ala277Val
ENST00000676439.1:n.1004C>T
ENST00000251127.10:c.830C>T	ENSP00000251127.6:p.Ala277Val
ENST00000470333.1:n.926C>T
ENST00000497170.5:n.984C>T
NM_052867.2:c.830C>T	NP_443099.1:p.Ala277Val
XM_011521067.1:c.887C>T	XP_011519369.1:p.Ala296Val
XM_011521068.1:c.830C>T	XP_011519370.1:p.Ala277Val
XM_011521069.1:c.887C>T	XP_011519371.1:p.Ala296Val
XM_011521070.1:c.887C>T	XP_011519372.1:p.Ala296Val
NM_001350748.1:c.830C>T	NP_001337677.1:p.Ala277Val
NM_001350749.1:c.830C>T	NP_001337678.1:p.Ala277Val
NM_001350750.1:c.830C>T	NP_001337679.1:p.Ala277Val
NM_001350751.1:c.830C>T	NP_001337680.1:p.Ala277Val
NM_052867.3:c.830C>T	NP_443099.1:p.Ala277Val
XM_011521067.2:c.887C>T	XP_011519369.1:p.Ala296Val
XM_011521069.2:c.887C>T	XP_011519371.1:p.Ala296Val
XM_017020536.2:c.383C>T	XP_016876025.1:p.Ala128Val
XM_017020537.1:c.65C>T	XP_016876026.1:p.Ala22Val
XM_024449336.1:c.887C>T	XP_024305104.1:p.Ala296Val
NM_052867.4:c.830C>T MANE Select	NP_443099.1:p.Ala277Val
NM_001350748.2:c.830C>T	NP_001337677.1:p.Ala277Val
NM_001350749.2:c.830C>T	NP_001337678.1:p.Ala277Val
NM_001350750.2:c.830C>T	NP_001337679.1:p.Ala277Val
NM_001350751.2:c.830C>T	NP_001337680.1:p.Ala277Val