Canonical Allele Identifier: CA388650429
Gene: NALCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.101081623C>A , CM000675.2:g.101081623C>A GRCh38
NC_000013.10:g.101733974C>A , CM000675.1:g.101733974C>A GRCh37
NC_000013.9:g.100531975C>A NCBI36
NG_053176.1:g.340584G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000251127.11:c.3789G>T MANE Select ENSP00000251127.6:p.Met1263Ile
ENST00000648359.1:c.3789G>T ENSP00000497465.1:p.Met1263Ile
ENST00000675150.1:c.3510G>T ENSP00000502680.1:p.Met1170Ile
ENST00000675332.1:c.3876G>T ENSP00000501955.1:p.Met1292Ile
ENST00000676315.1:c.3702G>T ENSP00000501603.1:p.Met1234Ile
ENST00000251127.10:c.3789G>T ENSP00000251127.6:p.Met1263Ile
NM_052867.2:c.3789G>T NP_443099.1:p.Met1263Ile
XM_011521067.1:c.3846G>T XP_011519369.1:p.Met1282Ile
XM_011521068.1:c.3789G>T XP_011519370.1:p.Met1263Ile
XM_011521069.1:c.3759G>T XP_011519371.1:p.Met1253Ile
XM_011521070.1:c.3567G>T XP_011519372.1:p.Met1189Ile
NM_001350748.1:c.3876G>T NP_001337677.1:p.Met1292Ile
NM_001350749.1:c.3789G>T NP_001337678.1:p.Met1263Ile
NM_001350750.1:c.3702G>T NP_001337679.1:p.Met1234Ile
NM_001350751.1:c.3702G>T NP_001337680.1:p.Met1234Ile
NM_052867.3:c.3789G>T NP_443099.1:p.Met1263Ile
XM_011521067.2:c.3846G>T XP_011519369.1:p.Met1282Ile
XM_011521069.2:c.3759G>T XP_011519371.1:p.Met1253Ile
XM_017020536.2:c.3342G>T XP_016876025.1:p.Met1114Ile
XM_017020537.1:c.3024G>T XP_016876026.1:p.Met1008Ile
XM_024449336.1:c.3933G>T XP_024305104.1:p.Met1311Ile
NM_052867.4:c.3789G>T MANE Select NP_443099.1:p.Met1263Ile
NM_001350748.2:c.3876G>T NP_001337677.1:p.Met1292Ile
NM_001350749.2:c.3789G>T NP_001337678.1:p.Met1263Ile
NM_001350750.2:c.3702G>T NP_001337679.1:p.Met1234Ile
NM_001350751.2:c.3702G>T NP_001337680.1:p.Met1234Ile