Canonical Allele Identifier: CA2114454997
Gene: NALCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101227237_101227238delinsGA , CM000675.2:g.101227237_101227238delinsGA GRCh38
NC_000013.10:g.101879588_101879589delinsGA , CM000675.1:g.101879588_101879589delinsGA GRCh37
NC_000013.9:g.100677589_100677590delinsGA NCBI36
NG_053176.1:g.194969_194970delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000251127.11:c.1626+2155_1626+2156delinsTC MANE Select ENSP00000251127.6:n.1626+2155_1626+2156de...
ENST00000648359.1:c.1626+2155_1626+2156delinsTC ENSP00000497465.1:n.1626+2155_1626+2156de...
ENST00000674840.1:n.1724+2155_1724+2156delinsTC
ENST00000674904.1:n.1706+2155_1706+2156delinsTC
ENST00000675150.1:c.1626+2155_1626+2156delinsTC ENSP00000502680.1:n.1626+2155_1626+2156de...
ENST00000675332.1:c.1626+2155_1626+2156delinsTC ENSP00000501955.1:n.1626+2155_1626+2156de...
ENST00000675594.1:c.*1063+2155_*1063+2156delinsTC ENSP00000502490.1:n.*1063+2155_*1063+2156...
ENST00000675802.1:c.1626+2155_1626+2156delinsTC ENSP00000501818.1:n.1626+2155_1626+2156de...
ENST00000676315.1:c.1539+2155_1539+2156delinsTC ENSP00000501603.1:n.1539+2155_1539+2156de...
ENST00000676439.1:n.1800+2155_1800+2156delinsTC
ENST00000251127.10:c.1626+2155_1626+2156delinsTC ENSP00000251127.6:n.1626+2155_1626+2156de...
ENST00000470333.1:n.1722+2155_1722+2156delinsTC
ENST00000497170.5:n.1780+2155_1780+2156delinsTC
NM_052867.2:c.1626+2155_1626+2156delinsTC NP_443099.1:n.1626+2155_1626+2156delinsTC...
XM_011521067.1:c.1683+2155_1683+2156delinsTC XP_011519369.1:n.1683+2155_1683+2156delin...
XM_011521068.1:c.1626+2155_1626+2156delinsTC XP_011519370.1:n.1626+2155_1626+2156delin...
XM_011521069.1:c.1596+2155_1596+2156delinsTC XP_011519371.1:n.1596+2155_1596+2156delin...
XM_011521070.1:c.1683+2155_1683+2156delinsTC XP_011519372.1:n.1683+2155_1683+2156delin...
NM_001350748.1:c.1626+2155_1626+2156delinsTC NP_001337677.1:n.1626+2155_1626+2156delin...
NM_001350749.1:c.1626+2155_1626+2156delinsTC NP_001337678.1:n.1626+2155_1626+2156delin...
NM_001350750.1:c.1539+2155_1539+2156delinsTC NP_001337679.1:n.1539+2155_1539+2156delin...
NM_001350751.1:c.1539+2155_1539+2156delinsTC NP_001337680.1:n.1539+2155_1539+2156delin...
NM_052867.3:c.1626+2155_1626+2156delinsTC NP_443099.1:n.1626+2155_1626+2156delinsTC...
XM_011521067.2:c.1683+2155_1683+2156delinsTC XP_011519369.1:n.1683+2155_1683+2156delin...
XM_011521069.2:c.1596+2155_1596+2156delinsTC XP_011519371.1:n.1596+2155_1596+2156delin...
XM_017020536.2:c.1179+2155_1179+2156delinsTC XP_016876025.1:n.1179+2155_1179+2156delin...
XM_017020537.1:c.861+2155_861+2156delinsTC XP_016876026.1:n.861+2155_861+2156delinsT...
XM_024449336.1:c.1683+2155_1683+2156delinsTC XP_024305104.1:n.1683+2155_1683+2156delin...
NM_052867.4:c.1626+2155_1626+2156delinsTC MANE Select NP_443099.1:n.1626+2155_1626+2156delinsTC...
NM_001350748.2:c.1626+2155_1626+2156delinsTC NP_001337677.1:n.1626+2155_1626+2156delin...
NM_001350749.2:c.1626+2155_1626+2156delinsTC NP_001337678.1:n.1626+2155_1626+2156delin...
NM_001350750.2:c.1539+2155_1539+2156delinsTC NP_001337679.1:n.1539+2155_1539+2156delin...
NM_001350751.2:c.1539+2155_1539+2156delinsTC NP_001337680.1:n.1539+2155_1539+2156delin...