Canonical Allele Identifier: CA2114522337

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101376729A= , CM000675.2:g.101376729A=	GRCh38
NC_000013.10:g.102029080A= , CM000675.1:g.102029080A=	GRCh37
NC_000013.9:g.100827081A=	NCBI36
NG_053176.1:g.45478T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.615T= MANE Select	ENSP00000251127.6:p.Tyr205=
ENST00000376200.6:c.615T=	ENSP00000365373.5:p.Tyr205=
ENST00000648359.1:c.615T=	ENSP00000497465.1:p.Tyr205=
ENST00000674840.1:n.713T=
ENST00000674904.1:n.695T=
ENST00000675150.1:c.615T=	ENSP00000502680.1:p.Tyr205=
ENST00000675332.1:c.615T=	ENSP00000501955.1:p.Tyr205=
ENST00000675415.1:n.798T=
ENST00000675594.1:c.615T=	ENSP00000502490.1:p.Tyr205=
ENST00000675802.1:c.615T=	ENSP00000501818.1:p.Tyr205=
ENST00000676315.1:c.615T=	ENSP00000501603.1:p.Tyr205=
ENST00000676357.1:n.835T=
ENST00000676439.1:n.789T=
ENST00000251127.10:c.615T=	ENSP00000251127.6:p.Tyr205=
ENST00000376200.5:c.615T=	ENSP00000365373.5:p.Tyr205=
ENST00000470333.1:n.711T=
ENST00000497170.5:n.804T=
NM_052867.2:c.615T=	NP_443099.1:p.Tyr205=
XM_011521067.1:c.672T=	XP_011519369.1:p.Tyr224=
XM_011521068.1:c.615T=	XP_011519370.1:p.Tyr205=
XM_011521069.1:c.672T=	XP_011519371.1:p.Tyr224=
XM_011521070.1:c.672T=	XP_011519372.1:p.Tyr224=
NM_001350748.1:c.615T=	NP_001337677.1:p.Tyr205=
NM_001350749.1:c.615T=	NP_001337678.1:p.Tyr205=
NM_001350750.1:c.615T=	NP_001337679.1:p.Tyr205=
NM_001350751.1:c.615T=	NP_001337680.1:p.Tyr205=
NM_052867.3:c.615T=	NP_443099.1:p.Tyr205=
XM_011521067.2:c.672T=	XP_011519369.1:p.Tyr224=
XM_011521069.2:c.672T=	XP_011519371.1:p.Tyr224=
XM_024449336.1:c.672T=	XP_024305104.1:p.Tyr224=
NM_052867.4:c.615T= MANE Select	NP_443099.1:p.Tyr205=
NM_001350748.2:c.615T=	NP_001337677.1:p.Tyr205=
NM_001350749.2:c.615T=	NP_001337678.1:p.Tyr205=
NM_001350750.2:c.615T=	NP_001337679.1:p.Tyr205=
NM_001350751.2:c.615T=	NP_001337680.1:p.Tyr205=