Canonical Allele Identifier: CA388650224

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733912C>T (hg19) ; chr13:g.101081561C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081561C>T , CM000675.2:g.101081561C>T	GRCh38
NC_000013.10:g.101733912C>T , CM000675.1:g.101733912C>T	GRCh37
NC_000013.9:g.100531913C>T	NCBI36
NG_053176.1:g.340646G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.3851G>A MANE Select	ENSP00000251127.6:p.Gly1284Asp
ENST00000648359.1:c.3851G>A	ENSP00000497465.1:p.Gly1284Asp
ENST00000675150.1:c.3572G>A	ENSP00000502680.1:p.Gly1191Asp
ENST00000675332.1:c.3938G>A	ENSP00000501955.1:p.Gly1313Asp
ENST00000676315.1:c.3764G>A	ENSP00000501603.1:p.Gly1255Asp
ENST00000251127.10:c.3851G>A	ENSP00000251127.6:p.Gly1284Asp
NM_052867.2:c.3851G>A	NP_443099.1:p.Gly1284Asp
XM_011521067.1:c.3908G>A	XP_011519369.1:p.Gly1303Asp
XM_011521068.1:c.3851G>A	XP_011519370.1:p.Gly1284Asp
XM_011521069.1:c.3821G>A	XP_011519371.1:p.Gly1274Asp
XM_011521070.1:c.3629G>A	XP_011519372.1:p.Gly1210Asp
NM_001350748.1:c.3938G>A	NP_001337677.1:p.Gly1313Asp
NM_001350749.1:c.3851G>A	NP_001337678.1:p.Gly1284Asp
NM_001350750.1:c.3764G>A	NP_001337679.1:p.Gly1255Asp
NM_001350751.1:c.3764G>A	NP_001337680.1:p.Gly1255Asp
NM_052867.3:c.3851G>A	NP_443099.1:p.Gly1284Asp
XM_011521067.2:c.3908G>A	XP_011519369.1:p.Gly1303Asp
XM_011521069.2:c.3821G>A	XP_011519371.1:p.Gly1274Asp
XM_017020536.2:c.3404G>A	XP_016876025.1:p.Gly1135Asp
XM_017020537.1:c.3086G>A	XP_016876026.1:p.Gly1029Asp
XM_024449336.1:c.3995G>A	XP_024305104.1:p.Gly1332Asp
NM_052867.4:c.3851G>A MANE Select	NP_443099.1:p.Gly1284Asp
NM_001350748.2:c.3938G>A	NP_001337677.1:p.Gly1313Asp
NM_001350749.2:c.3851G>A	NP_001337678.1:p.Gly1284Asp
NM_001350750.2:c.3764G>A	NP_001337679.1:p.Gly1255Asp
NM_001350751.2:c.3764G>A	NP_001337680.1:p.Gly1255Asp