Canonical Allele Identifier: CA2523853089

Gene: NALCN

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101227166_101227167del , CM000675.2:g.101227166_101227167del	GRCh38
NC_000013.10:g.101879517_101879518del , CM000675.1:g.101879517_101879518del	GRCh37
NC_000013.9:g.100677518_100677519del	NCBI36
NG_053176.1:g.195040_195041del

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.1626+2226_1626+2227del MANE Select	ENSP00000251127.6:n.1626+2226_1626+2227de...
ENST00000648359.1:c.1626+2226_1626+2227del	ENSP00000497465.1:n.1626+2226_1626+2227de...
ENST00000674840.1:n.1724+2226_1724+2227del
ENST00000674904.1:n.1706+2226_1706+2227del
ENST00000675150.1:c.1626+2226_1626+2227del	ENSP00000502680.1:n.1626+2226_1626+2227de...
ENST00000675332.1:c.1626+2226_1626+2227del	ENSP00000501955.1:n.1626+2226_1626+2227de...
ENST00000675594.1:c.*1063+2226_*1063+2227del	ENSP00000502490.1:n.*1063+2226_*1063+2227...
ENST00000675802.1:c.1626+2226_1626+2227del	ENSP00000501818.1:n.1626+2226_1626+2227de...
ENST00000676315.1:c.1539+2226_1539+2227del	ENSP00000501603.1:n.1539+2226_1539+2227de...
ENST00000676439.1:n.1800+2226_1800+2227del
ENST00000251127.10:c.1626+2226_1626+2227del	ENSP00000251127.6:n.1626+2226_1626+2227de...
ENST00000470333.1:n.1722+2226_1722+2227del
ENST00000497170.5:n.1780+2226_1780+2227del
NM_052867.2:c.1626+2226_1626+2227del	NP_443099.1:n.1626+2226_1626+2227del
XM_011521067.1:c.1683+2226_1683+2227del	XP_011519369.1:n.1683+2226_1683+2227del
XM_011521068.1:c.1626+2226_1626+2227del	XP_011519370.1:n.1626+2226_1626+2227del
XM_011521069.1:c.1596+2226_1596+2227del	XP_011519371.1:n.1596+2226_1596+2227del
XM_011521070.1:c.1683+2226_1683+2227del	XP_011519372.1:n.1683+2226_1683+2227del
NM_001350748.1:c.1626+2226_1626+2227del	NP_001337677.1:n.1626+2226_1626+2227del
NM_001350749.1:c.1626+2226_1626+2227del	NP_001337678.1:n.1626+2226_1626+2227del
NM_001350750.1:c.1539+2226_1539+2227del	NP_001337679.1:n.1539+2226_1539+2227del
NM_001350751.1:c.1539+2226_1539+2227del	NP_001337680.1:n.1539+2226_1539+2227del
NM_052867.3:c.1626+2226_1626+2227del	NP_443099.1:n.1626+2226_1626+2227del
XM_011521067.2:c.1683+2226_1683+2227del	XP_011519369.1:n.1683+2226_1683+2227del
XM_011521069.2:c.1596+2226_1596+2227del	XP_011519371.1:n.1596+2226_1596+2227del
XM_017020536.2:c.1179+2226_1179+2227del	XP_016876025.1:n.1179+2226_1179+2227del
XM_017020537.1:c.861+2226_861+2227del	XP_016876026.1:n.861+2226_861+2227del
XM_024449336.1:c.1683+2226_1683+2227del	XP_024305104.1:n.1683+2226_1683+2227del
NM_052867.4:c.1626+2226_1626+2227del MANE Select	NP_443099.1:n.1626+2226_1626+2227del
NM_001350748.2:c.1626+2226_1626+2227del	NP_001337677.1:n.1626+2226_1626+2227del
NM_001350749.2:c.1626+2226_1626+2227del	NP_001337678.1:n.1626+2226_1626+2227del
NM_001350750.2:c.1539+2226_1539+2227del	NP_001337679.1:n.1539+2226_1539+2227del
NM_001350751.2:c.1539+2226_1539+2227del	NP_001337680.1:n.1539+2226_1539+2227del