Canonical Allele Identifier: CA388669201

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101755563A>C (hg19) ; chr13:g.101103212A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101103212A>C , CM000675.2:g.101103212A>C	GRCh38
NC_000013.10:g.101755563A>C , CM000675.1:g.101755563A>C	GRCh37
NC_000013.9:g.100553564A>C	NCBI36
NG_053176.1:g.318995T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.3017T>G MANE Select	ENSP00000251127.6:p.Val1006Gly
ENST00000648359.1:c.3017T>G	ENSP00000497465.1:p.Val1006Gly
ENST00000675150.1:c.2738T>G	ENSP00000502680.1:p.Val913Gly
ENST00000675332.1:c.3104T>G	ENSP00000501955.1:p.Val1035Gly
ENST00000676315.1:c.2930T>G	ENSP00000501603.1:p.Val977Gly
ENST00000251127.10:c.3017T>G	ENSP00000251127.6:p.Val1006Gly
NM_052867.2:c.3017T>G	NP_443099.1:p.Val1006Gly
XM_011521067.1:c.3074T>G	XP_011519369.1:p.Val1025Gly
XM_011521068.1:c.3017T>G	XP_011519370.1:p.Val1006Gly
XM_011521069.1:c.2987T>G	XP_011519371.1:p.Val996Gly
XM_011521070.1:c.2795T>G	XP_011519372.1:p.Val932Gly
NM_001350748.1:c.3104T>G	NP_001337677.1:p.Val1035Gly
NM_001350749.1:c.3017T>G	NP_001337678.1:p.Val1006Gly
NM_001350750.1:c.2930T>G	NP_001337679.1:p.Val977Gly
NM_001350751.1:c.2930T>G	NP_001337680.1:p.Val977Gly
NM_052867.3:c.3017T>G	NP_443099.1:p.Val1006Gly
XM_011521067.2:c.3074T>G	XP_011519369.1:p.Val1025Gly
XM_011521069.2:c.2987T>G	XP_011519371.1:p.Val996Gly
XM_017020536.2:c.2570T>G	XP_016876025.1:p.Val857Gly
XM_017020537.1:c.2252T>G	XP_016876026.1:p.Val751Gly
XM_024449336.1:c.3161T>G	XP_024305104.1:p.Val1054Gly
NM_052867.4:c.3017T>G MANE Select	NP_443099.1:p.Val1006Gly
NM_001350748.2:c.3104T>G	NP_001337677.1:p.Val1035Gly
NM_001350749.2:c.3017T>G	NP_001337678.1:p.Val1006Gly
NM_001350750.2:c.2930T>G	NP_001337679.1:p.Val977Gly
NM_001350751.2:c.2930T>G	NP_001337680.1:p.Val977Gly