Canonical Allele Identifier: CA2114379336
Gene: NALCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101060994_101060997delinsCGTT , CM000675.2:g.101060994_101060997delinsCGTT GRCh38
NC_000013.10:g.101713346_101713349delinsCGTT , CM000675.1:g.101713346_101713349delinsCGTT GRCh37
NC_000013.9:g.100511347_100511350delinsCGTT NCBI36
NG_053176.1:g.361210_361213delinsAACG

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.4755+971_4755+974delinsAACG MANE Select ENSP00000251127.6:n.4755+971_4755+974deli...
ENST00000648359.1:c.*375+971_*375+974delinsAACG ENSP00000497465.1:n.*375+971_*375+974deli...
ENST00000675150.1:c.4476+971_4476+974delinsAACG ENSP00000502680.1:n.4476+971_4476+974deli...
ENST00000675332.1:c.4842+971_4842+974delinsAACG ENSP00000501955.1:n.4842+971_4842+974deli...
ENST00000676315.1:c.4668+971_4668+974delinsAACG ENSP00000501603.1:n.4668+971_4668+974deli...
ENST00000251127.10:c.4755+971_4755+974delinsAACG ENSP00000251127.6:n.4755+971_4755+974deli...
NM_052867.2:c.4755+971_4755+974delinsAACG NP_443099.1:n.4755+971_4755+974delinsAACG...
XM_011521067.1:c.4812+971_4812+974delinsAACG XP_011519369.1:n.4812+971_4812+974delinsA...
XM_011521068.1:c.4755+971_4755+974delinsAACG XP_011519370.1:n.4755+971_4755+974delinsA...
XM_011521069.1:c.4725+971_4725+974delinsAACG XP_011519371.1:n.4725+971_4725+974delinsA...
XM_011521070.1:c.4533+971_4533+974delinsAACG XP_011519372.1:n.4533+971_4533+974delinsA...
NM_001350748.1:c.4842+971_4842+974delinsAACG NP_001337677.1:n.4842+971_4842+974delinsA...
NM_001350749.1:c.4755+971_4755+974delinsAACG NP_001337678.1:n.4755+971_4755+974delinsA...
NM_001350750.1:c.4668+971_4668+974delinsAACG NP_001337679.1:n.4668+971_4668+974delinsA...
NM_001350751.1:c.4668+971_4668+974delinsAACG NP_001337680.1:n.4668+971_4668+974delinsA...
NM_052867.3:c.4755+971_4755+974delinsAACG NP_443099.1:n.4755+971_4755+974delinsAACG...
XM_011521067.2:c.4812+971_4812+974delinsAACG XP_011519369.1:n.4812+971_4812+974delinsA...
XM_011521069.2:c.4725+971_4725+974delinsAACG XP_011519371.1:n.4725+971_4725+974delinsA...
XM_017020536.2:c.4308+971_4308+974delinsAACG XP_016876025.1:n.4308+971_4308+974delinsA...
XM_017020537.1:c.3990+971_3990+974delinsAACG XP_016876026.1:n.3990+971_3990+974delinsA...
XM_024449336.1:c.4899+971_4899+974delinsAACG XP_024305104.1:n.4899+971_4899+974delinsA...
NM_052867.4:c.4755+971_4755+974delinsAACG MANE Select NP_443099.1:n.4755+971_4755+974delinsAACG...
NM_001350748.2:c.4842+971_4842+974delinsAACG NP_001337677.1:n.4842+971_4842+974delinsA...
NM_001350749.2:c.4755+971_4755+974delinsAACG NP_001337678.1:n.4755+971_4755+974delinsA...
NM_001350750.2:c.4668+971_4668+974delinsAACG NP_001337679.1:n.4668+971_4668+974delinsA...
NM_001350751.2:c.4668+971_4668+974delinsAACG NP_001337680.1:n.4668+971_4668+974delinsA...