Canonical Allele Identifier: CA1139968037

Gene: NRDC

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.51858556C= , CM000663.2:g.51858556C=	GRCh38
NC_000001.10:g.52324228C= , CM000663.1:g.52324228C=	GRCh37
NC_000001.9:g.52096816C=	NCBI36
NG_029171.1:g.25382G=
NG_029171.2:g.25382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000352171.12:c.342-18042G= MANE Select	ENSP00000262679.8:n.342-18042G=
ENST00000352171.11:c.342-18042G=	ENSP00000262679.8:n.342-18042G=
ENST00000354831.11:c.342-18042G=	ENSP00000346890.7:n.342-18042G=
ENST00000491410.1:n.498-18042G=
ENST00000539524.5:c.-55-18042G=	ENSP00000444416.1:n.-55-18042G=
ENST00000544028.5:c.342-18042G=	ENSP00000442262.2:n.342-18042G=
ENST00000615102.1:c.342-18042G=	ENSP00000481902.1:n.342-18042G=
NM_001101662.1:c.342-18042G=	NP_001095132.1:n.342-18042G=
NM_001242361.1:c.-55-18042G=	NP_001229290.1:n.-55-18042G=
NM_002525.2:c.342-18042G=	NP_002516.2:n.342-18042G=
XM_011541521.1:c.342-18042G=	XP_011539823.1:n.342-18042G=
XM_011541522.1:c.-152-3168G=	XP_011539824.1:n.-152-3168G=
XM_011541523.1:c.-55-18042G=	XP_011539825.1:n.-55-18042G=
XM_011541524.1:c.342-18042G=	XP_011539826.1:n.342-18042G=
XR_946660.1:n.532-18042G=
XM_011541525.2:c.-605-18042G=	XP_011539827.1:n.-605-18042G=
XM_017001375.1:c.-55-18042G=	XP_016856864.1:n.-55-18042G=
XM_024447364.1:c.-55-18042G=	XP_024303132.1:n.-55-18042G=
XM_024447365.1:c.-440-18042G=	XP_024303133.1:n.-440-18042G=
NM_001101662.2:c.342-18042G= MANE Select	NP_001095132.1:n.342-18042G=
NM_001242361.2:c.-55-18042G=	NP_001229290.1:n.-55-18042G=
NM_002525.3:c.342-18042G=	NP_002516.2:n.342-18042G=