Canonical Allele Identifier: CA2114388897
Gene: NALCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101081721_101081722delinsAT , CM000675.2:g.101081721_101081722delinsAT GRCh38
NC_000013.10:g.101734072_101734073delinsAT , CM000675.1:g.101734072_101734073delinsAT GRCh37
NC_000013.9:g.100532073_100532074delinsAT NCBI36
NG_053176.1:g.340485_340486delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000251127.11:c.3766-76_3766-75delinsAT MANE Select ENSP00000251127.6:n.3766-76_3766-75delinsAT
ENST00000648359.1:c.3766-76_3766-75delinsAT ENSP00000497465.1:n.3766-76_3766-75delinsAT
ENST00000675150.1:c.3487-76_3487-75delinsAT ENSP00000502680.1:n.3487-76_3487-75delinsAT
ENST00000675332.1:c.3853-76_3853-75delinsAT ENSP00000501955.1:n.3853-76_3853-75delinsAT
ENST00000676315.1:c.3679-76_3679-75delinsAT ENSP00000501603.1:n.3679-76_3679-75delinsAT
ENST00000251127.10:c.3766-76_3766-75delinsAT ENSP00000251127.6:n.3766-76_3766-75delinsAT
NM_052867.2:c.3766-76_3766-75delinsAT NP_443099.1:n.3766-76_3766-75delinsAT
XM_011521067.1:c.3823-76_3823-75delinsAT XP_011519369.1:n.3823-76_3823-75delinsAT
XM_011521068.1:c.3766-76_3766-75delinsAT XP_011519370.1:n.3766-76_3766-75delinsAT
XM_011521069.1:c.3736-76_3736-75delinsAT XP_011519371.1:n.3736-76_3736-75delinsAT
XM_011521070.1:c.3544-76_3544-75delinsAT XP_011519372.1:n.3544-76_3544-75delinsAT
NM_001350748.1:c.3853-76_3853-75delinsAT NP_001337677.1:n.3853-76_3853-75delinsAT
NM_001350749.1:c.3766-76_3766-75delinsAT NP_001337678.1:n.3766-76_3766-75delinsAT
NM_001350750.1:c.3679-76_3679-75delinsAT NP_001337679.1:n.3679-76_3679-75delinsAT
NM_001350751.1:c.3679-76_3679-75delinsAT NP_001337680.1:n.3679-76_3679-75delinsAT
NM_052867.3:c.3766-76_3766-75delinsAT NP_443099.1:n.3766-76_3766-75delinsAT
XM_011521067.2:c.3823-76_3823-75delinsAT XP_011519369.1:n.3823-76_3823-75delinsAT
XM_011521069.2:c.3736-76_3736-75delinsAT XP_011519371.1:n.3736-76_3736-75delinsAT
XM_017020536.2:c.3319-76_3319-75delinsAT XP_016876025.1:n.3319-76_3319-75delinsAT
XM_017020537.1:c.3001-76_3001-75delinsAT XP_016876026.1:n.3001-76_3001-75delinsAT
XM_024449336.1:c.3910-76_3910-75delinsAT XP_024305104.1:n.3910-76_3910-75delinsAT
NM_052867.4:c.3766-76_3766-75delinsAT MANE Select NP_443099.1:n.3766-76_3766-75delinsAT
NM_001350748.2:c.3853-76_3853-75delinsAT NP_001337677.1:n.3853-76_3853-75delinsAT
NM_001350749.2:c.3766-76_3766-75delinsAT NP_001337678.1:n.3766-76_3766-75delinsAT
NM_001350750.2:c.3679-76_3679-75delinsAT NP_001337679.1:n.3679-76_3679-75delinsAT
NM_001350751.2:c.3679-76_3679-75delinsAT NP_001337680.1:n.3679-76_3679-75delinsAT