Canonical Allele Identifier: CA388704640
Gene: NALCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101291998T>G , CM000675.2:g.101291998T>G GRCh38
NC_000013.10:g.101944349T>G , CM000675.1:g.101944349T>G GRCh37
NC_000013.9:g.100742350T>G NCBI36
NG_053176.1:g.130209A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000251127.11:c.1039A>C MANE Select ENSP00000251127.6:p.Thr347Pro
ENST00000648359.1:c.1039A>C ENSP00000497465.1:p.Thr347Pro
ENST00000674840.1:n.1137A>C
ENST00000674904.1:n.1119A>C
ENST00000675150.1:c.1039A>C ENSP00000502680.1:p.Thr347Pro
ENST00000675332.1:c.1039A>C ENSP00000501955.1:p.Thr347Pro
ENST00000675415.1:n.1222A>C
ENST00000675594.1:c.*476A>C ENSP00000502490.1:n.*476A>C
ENST00000675802.1:c.1039A>C ENSP00000501818.1:p.Thr347Pro
ENST00000676315.1:c.1039A>C ENSP00000501603.1:p.Thr347Pro
ENST00000676439.1:n.1213A>C
ENST00000251127.10:c.1039A>C ENSP00000251127.6:p.Thr347Pro
ENST00000470333.1:n.1135A>C
ENST00000497170.5:n.1193A>C
NM_052867.2:c.1039A>C NP_443099.1:p.Thr347Pro
XM_011521067.1:c.1096A>C XP_011519369.1:p.Thr366Pro
XM_011521068.1:c.1039A>C XP_011519370.1:p.Thr347Pro
XM_011521069.1:c.1096A>C XP_011519371.1:p.Thr366Pro
XM_011521070.1:c.1096A>C XP_011519372.1:p.Thr366Pro
NM_001350748.1:c.1039A>C NP_001337677.1:p.Thr347Pro
NM_001350749.1:c.1039A>C NP_001337678.1:p.Thr347Pro
NM_001350750.1:c.1039A>C NP_001337679.1:p.Thr347Pro
NM_001350751.1:c.1039A>C NP_001337680.1:p.Thr347Pro
NM_052867.3:c.1039A>C NP_443099.1:p.Thr347Pro
XM_011521067.2:c.1096A>C XP_011519369.1:p.Thr366Pro
XM_011521069.2:c.1096A>C XP_011519371.1:p.Thr366Pro
XM_017020536.2:c.592A>C XP_016876025.1:p.Thr198Pro
XM_017020537.1:c.274A>C XP_016876026.1:p.Thr92Pro
XM_024449336.1:c.1096A>C XP_024305104.1:p.Thr366Pro
NM_052867.4:c.1039A>C MANE Select NP_443099.1:p.Thr347Pro
NM_001350748.2:c.1039A>C NP_001337677.1:p.Thr347Pro
NM_001350749.2:c.1039A>C NP_001337678.1:p.Thr347Pro
NM_001350750.2:c.1039A>C NP_001337679.1:p.Thr347Pro
NM_001350751.2:c.1039A>C NP_001337680.1:p.Thr347Pro