Canonical Allele Identifier: CA2580602918
Community Standard Title: NM_052867.4(NALCN):c.5024-470C>G
Gene: NALCN HGNC NCBI
NALCN-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101055958G>C , CM000675.2:g.101055958G>C GRCh38
NC_000013.10:g.101708310G>C , CM000675.1:g.101708310G>C GRCh37
NC_000013.9:g.100506311G>C NCBI36
NG_053176.1:g.366249C>G

Transcript Alleles

HGVS Amino-acid Change
NM_052867.4:c.5024-470C>G (NALCN) MANE Select NP_443099.1:n.5024-470C>G
ENST00000251127.11:c.5024-470C>G (NALCN) MANE Select ENSP00000251127.6:n.5024-470C>G
NM_001350748.1:c.5111-470C>G (NALCN) NP_001337677.1:n.5111-470C>G
NM_001350748.2:c.5111-470C>G (NALCN) NP_001337677.1:n.5111-470C>G
NM_001350749.1:c.5024-470C>G (NALCN) NP_001337678.1:n.5024-470C>G
NM_001350749.2:c.5024-470C>G (NALCN) NP_001337678.1:n.5024-470C>G
NM_001350750.1:c.4937-470C>G (NALCN) NP_001337679.1:n.4937-470C>G
NM_001350750.2:c.4937-470C>G (NALCN) NP_001337679.1:n.4937-470C>G
NM_001350751.1:c.4937-470C>G (NALCN) NP_001337680.1:n.4937-470C>G
NM_001350751.2:c.4937-470C>G (NALCN) NP_001337680.1:n.4937-470C>G
NM_052867.2:c.5024-470C>G (NALCN) NP_443099.1:n.5024-470C>G
NM_052867.3:c.5024-470C>G (NALCN) NP_443099.1:n.5024-470C>G
NR_047687.1:n.770+512G>C (NALCN-AS1)
ENST00000251127.10:c.5024-470C>G (NALCN) ENSP00000251127.6:n.5024-470C>G
ENST00000648359.1:c.*644-470C>G (NALCN) ENSP00000497465.1:n.*644-470C>G
ENST00000675150.1:c.4745-470C>G (NALCN) ENSP00000502680.1:n.4745-470C>G
ENST00000675332.1:c.5111-470C>G (NALCN) ENSP00000501955.1:n.5111-470C>G
ENST00000676315.1:c.4937-470C>G (NALCN) ENSP00000501603.1:n.4937-470C>G
XM_011521067.1:c.5081-470C>G (NALCN) XP_011519369.1:n.5081-470C>G
XM_011521067.2:c.5081-470C>G (NALCN) XP_011519369.1:n.5081-470C>G
XM_011521068.1:c.5024-470C>G (NALCN) XP_011519370.1:n.5024-470C>G
XM_011521069.1:c.4994-470C>G (NALCN) XP_011519371.1:n.4994-470C>G
XM_011521069.2:c.4994-470C>G (NALCN) XP_011519371.1:n.4994-470C>G
XM_011521070.1:c.4802-470C>G (NALCN) XP_011519372.1:n.4802-470C>G
XM_017020536.2:c.4577-470C>G (NALCN) XP_016876025.1:n.4577-470C>G
XM_017020537.1:c.4259-470C>G (NALCN) XP_016876026.1:n.4259-470C>G
XM_024449336.1:c.5168-470C>G (NALCN) XP_024305104.1:n.5168-470C>G