Canonical Allele Identifier: CA484553414

Gene: NALCN

Linked Data

• MyVariant Identifiers: chr13:g.101736111C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.101083760C>A , CM000675.2:g.101083760C>A	GRCh38
NC_000013.10:g.101736111C>A , CM000675.1:g.101736111C>A	GRCh37
NC_000013.9:g.100534112C>A	NCBI36
NG_053176.1:g.338447G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000251127.11:c.3534G>T MANE Select	ENSP00000251127.6:p.Leu1178=
ENST00000648359.1:c.3534G>T	ENSP00000497465.1:p.Leu1178=
ENST00000675150.1:c.3255G>T	ENSP00000502680.1:p.Leu1085=
ENST00000675332.1:c.3621G>T	ENSP00000501955.1:p.Leu1207=
ENST00000676315.1:c.3447G>T	ENSP00000501603.1:p.Leu1149=
ENST00000251127.10:c.3534G>T	ENSP00000251127.6:p.Leu1178=
NM_052867.2:c.3534G>T	NP_443099.1:p.Leu1178=
XM_011521067.1:c.3591G>T	XP_011519369.1:p.Leu1197=
XM_011521068.1:c.3534G>T	XP_011519370.1:p.Leu1178=
XM_011521069.1:c.3504G>T	XP_011519371.1:p.Leu1168=
XM_011521070.1:c.3312G>T	XP_011519372.1:p.Leu1104=
NM_001350748.1:c.3621G>T	NP_001337677.1:p.Leu1207=
NM_001350749.1:c.3534G>T	NP_001337678.1:p.Leu1178=
NM_001350750.1:c.3447G>T	NP_001337679.1:p.Leu1149=
NM_001350751.1:c.3447G>T	NP_001337680.1:p.Leu1149=
NM_052867.3:c.3534G>T	NP_443099.1:p.Leu1178=
XM_011521067.2:c.3591G>T	XP_011519369.1:p.Leu1197=
XM_011521069.2:c.3504G>T	XP_011519371.1:p.Leu1168=
XM_017020536.2:c.3087G>T	XP_016876025.1:p.Leu1029=
XM_017020537.1:c.2769G>T	XP_016876026.1:p.Leu923=
XM_024449336.1:c.3678G>T	XP_024305104.1:p.Leu1226=
NM_052867.4:c.3534G>T MANE Select	NP_443099.1:p.Leu1178=
NM_001350748.2:c.3621G>T	NP_001337677.1:p.Leu1207=
NM_001350749.2:c.3534G>T	NP_001337678.1:p.Leu1178=
NM_001350750.2:c.3447G>T	NP_001337679.1:p.Leu1149=
NM_001350751.2:c.3447G>T	NP_001337680.1:p.Leu1149=