Canonical Allele Identifier: CA16479776

Gene: NALCN

Linked Data

• dbSNP Id: rs1338041
• gnomAD v2: 13-102058862-A-C
• gnomAD v3: 13-101406511-A-C
• gnomAD v4: 13-101406511-A-C
• MyVariant Identifiers: chr13:g.102058862A>C (hg19) ; chr13:g.101406511A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101406511A>C , CM000675.2:g.101406511A>C	GRCh38
NC_000013.10:g.102058862A>C , CM000675.1:g.102058862A>C	GRCh37
NC_000013.9:g.100856863A>C	NCBI36
NG_053176.1:g.15696T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.-39-7346T>G MANE Select	ENSP00000251127.6:n.-39-7346T>G
ENST00000648359.1:c.-39-7346T>G	ENSP00000497465.1:n.-39-7346T>G
ENST00000674840.1:n.60-7346T>G
ENST00000674904.1:n.126-7346T>G
ENST00000675150.1:c.-39-7346T>G	ENSP00000502680.1:n.-39-7346T>G
ENST00000675332.1:c.-39-7346T>G	ENSP00000501955.1:n.-39-7346T>G
ENST00000675415.1:n.145-7346T>G
ENST00000675802.1:c.-39-7346T>G	ENSP00000501818.1:n.-39-7346T>G
ENST00000676315.1:c.-39-7346T>G	ENSP00000501603.1:n.-39-7346T>G
ENST00000676357.1:n.182-7346T>G
ENST00000676439.1:n.136-7346T>G
ENST00000251127.10:c.-39-7346T>G	ENSP00000251127.6:n.-39-7346T>G
ENST00000470333.1:n.58-7346T>G
ENST00000497170.5:n.151-7346T>G
NM_052867.2:c.-39-7346T>G	NP_443099.1:n.-39-7346T>G
XM_011521067.1:c.19-7346T>G	XP_011519369.1:n.19-7346T>G
XM_011521068.1:c.-39-7346T>G	XP_011519370.1:n.-39-7346T>G
XM_011521069.1:c.19-7346T>G	XP_011519371.1:n.19-7346T>G
XM_011521070.1:c.19-7346T>G	XP_011519372.1:n.19-7346T>G
NM_001350748.1:c.-39-7346T>G	NP_001337677.1:n.-39-7346T>G
NM_001350749.1:c.-39-7346T>G	NP_001337678.1:n.-39-7346T>G
NM_001350750.1:c.-39-7346T>G	NP_001337679.1:n.-39-7346T>G
NM_001350751.1:c.-39-7346T>G	NP_001337680.1:n.-39-7346T>G
NM_052867.3:c.-39-7346T>G	NP_443099.1:n.-39-7346T>G
XM_011521067.2:c.19-7346T>G	XP_011519369.1:n.19-7346T>G
XM_011521069.2:c.19-7346T>G	XP_011519371.1:n.19-7346T>G
XM_024449336.1:c.19-7346T>G	XP_024305104.1:n.19-7346T>G
NM_052867.4:c.-39-7346T>G MANE Select	NP_443099.1:n.-39-7346T>G
NM_001350748.2:c.-39-7346T>G	NP_001337677.1:n.-39-7346T>G
NM_001350749.2:c.-39-7346T>G	NP_001337678.1:n.-39-7346T>G
NM_001350750.2:c.-39-7346T>G	NP_001337679.1:n.-39-7346T>G
NM_001350751.2:c.-39-7346T>G	NP_001337680.1:n.-39-7346T>G