Canonical Allele Identifier: CA388671770
Gene: NALCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101144823G>C , CM000675.2:g.101144823G>C GRCh38
NC_000013.10:g.101797174G>C , CM000675.1:g.101797174G>C GRCh37
NC_000013.9:g.100595175G>C NCBI36
NG_053176.1:g.277384C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.1913C>G MANE Select ENSP00000251127.6:p.Pro638Arg
ENST00000467264.2:c.105C>G
ENST00000648359.1:c.1913C>G ENSP00000497465.1:p.Pro638Arg
ENST00000675150.1:c.1840-20142C>G ENSP00000502680.1:n.1840-20142C>G
ENST00000675332.1:c.1913C>G ENSP00000501955.1:p.Pro638Arg
ENST00000675802.1:c.1913C>G ENSP00000501818.1:p.Pro638Arg
ENST00000676315.1:c.1826C>G ENSP00000501603.1:p.Pro609Arg
ENST00000251127.10:c.1913C>G ENSP00000251127.6:p.Pro638Arg
ENST00000497170.5:n.2067C>G
NM_052867.2:c.1913C>G NP_443099.1:p.Pro638Arg
XM_011521067.1:c.1970C>G XP_011519369.1:p.Pro657Arg
XM_011521068.1:c.1913C>G XP_011519370.1:p.Pro638Arg
XM_011521069.1:c.1883C>G XP_011519371.1:p.Pro628Arg
XM_011521070.1:c.1897-20142C>G XP_011519372.1:n.1897-20142C>G
NM_001350748.1:c.1913C>G NP_001337677.1:p.Pro638Arg
NM_001350749.1:c.1913C>G NP_001337678.1:p.Pro638Arg
NM_001350750.1:c.1826C>G NP_001337679.1:p.Pro609Arg
NM_001350751.1:c.1826C>G NP_001337680.1:p.Pro609Arg
NM_052867.3:c.1913C>G NP_443099.1:p.Pro638Arg
XM_011521067.2:c.1970C>G XP_011519369.1:p.Pro657Arg
XM_011521069.2:c.1883C>G XP_011519371.1:p.Pro628Arg
XM_017020536.2:c.1466C>G XP_016876025.1:p.Pro489Arg
XM_017020537.1:c.1148C>G XP_016876026.1:p.Pro383Arg
XM_024449336.1:c.1970C>G XP_024305104.1:p.Pro657Arg
NM_052867.4:c.1913C>G MANE Select NP_443099.1:p.Pro638Arg
NM_001350748.2:c.1913C>G NP_001337677.1:p.Pro638Arg
NM_001350749.2:c.1913C>G NP_001337678.1:p.Pro638Arg
NM_001350750.2:c.1826C>G NP_001337679.1:p.Pro609Arg
NM_001350751.2:c.1826C>G NP_001337680.1:p.Pro609Arg