Canonical Allele Identifier: CA388650184

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101733900A>G (hg19) ; chr13:g.101081549A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101081549A>G , CM000675.2:g.101081549A>G	GRCh38
NC_000013.10:g.101733900A>G , CM000675.1:g.101733900A>G	GRCh37
NC_000013.9:g.100531901A>G	NCBI36
NG_053176.1:g.340658T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000251127.11:c.3863T>C MANE Select	ENSP00000251127.6:p.Val1288Ala
ENST00000648359.1:c.3863T>C	ENSP00000497465.1:p.Val1288Ala
ENST00000675150.1:c.3584T>C	ENSP00000502680.1:p.Val1195Ala
ENST00000675332.1:c.3950T>C	ENSP00000501955.1:p.Val1317Ala
ENST00000676315.1:c.3776T>C	ENSP00000501603.1:p.Val1259Ala
ENST00000251127.10:c.3863T>C	ENSP00000251127.6:p.Val1288Ala
NM_052867.2:c.3863T>C	NP_443099.1:p.Val1288Ala
XM_011521067.1:c.3920T>C	XP_011519369.1:p.Val1307Ala
XM_011521068.1:c.3863T>C	XP_011519370.1:p.Val1288Ala
XM_011521069.1:c.3833T>C	XP_011519371.1:p.Val1278Ala
XM_011521070.1:c.3641T>C	XP_011519372.1:p.Val1214Ala
NM_001350748.1:c.3950T>C	NP_001337677.1:p.Val1317Ala
NM_001350749.1:c.3863T>C	NP_001337678.1:p.Val1288Ala
NM_001350750.1:c.3776T>C	NP_001337679.1:p.Val1259Ala
NM_001350751.1:c.3776T>C	NP_001337680.1:p.Val1259Ala
NM_052867.3:c.3863T>C	NP_443099.1:p.Val1288Ala
XM_011521067.2:c.3920T>C	XP_011519369.1:p.Val1307Ala
XM_011521069.2:c.3833T>C	XP_011519371.1:p.Val1278Ala
XM_017020536.2:c.3416T>C	XP_016876025.1:p.Val1139Ala
XM_017020537.1:c.3098T>C	XP_016876026.1:p.Val1033Ala
XM_024449336.1:c.4007T>C	XP_024305104.1:p.Val1336Ala
NM_052867.4:c.3863T>C MANE Select	NP_443099.1:p.Val1288Ala
NM_001350748.2:c.3950T>C	NP_001337677.1:p.Val1317Ala
NM_001350749.2:c.3863T>C	NP_001337678.1:p.Val1288Ala
NM_001350750.2:c.3776T>C	NP_001337679.1:p.Val1259Ala
NM_001350751.2:c.3776T>C	NP_001337680.1:p.Val1259Ala