Canonical Allele Identifier: CA10837909

Gene: NRDC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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