Canonical Allele Identifier: CA359522843

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064849G>C (hg19) ; chr5:g.37064747G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064747G>C , CM000667.2:g.37064747G>C	GRCh38
NC_000005.9:g.37064849G>C , CM000667.1:g.37064849G>C	GRCh37
NC_000005.8:g.37100606G>C	NCBI36
NG_006987.1:g.192865G>C
NG_006987.2:g.192865G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8270G>C (NIPBL) MANE Select	ENSP00000282516.8:p.Arg2757Pro
ENST00000652901.1:c.*214G>C (NIPBL)	ENSP00000499536.1:n.*214G>C
ENST00000282516.12:c.8270G>C (NIPBL)	ENSP00000282516.8:p.Arg2757Pro
ENST00000514335.1:n.2193G>C (NIPBL)
ENST00000621733.1:c.170G>C (NIPBL)	ENSP00000480694.1:p.Arg57Pro
NM_015384.4:c.*724G>C (NIPBL)	NP_056199.2:n.*724G>C
NM_133433.3:c.8270G>C (NIPBL)	NP_597677.2:p.Arg2757Pro
XM_005248280.2:c.*214G>C (NIPBL)	XP_005248337.1:n.*214G>C
XM_005248282.3:c.7526G>C (NIPBL)	XP_005248339.2:p.Arg2509Pro
XM_006714467.2:c.8123G>C (NIPBL)	XP_006714530.1:p.Arg2708Pro
XM_006714468.1:c.8072G>C (NIPBL)	XP_006714531.1:p.Arg2691Pro
XM_011514014.1:c.7889G>C (NIPBL)	XP_011512316.1:p.Arg2630Pro
XM_005248280.3:c.*214G>C (NIPBL)	XP_005248337.1:n.*214G>C
XM_005248282.5:c.7610G>C (NIPBL)	XP_005248339.3:p.Arg2537Pro
XM_006714468.2:c.8072G>C (NIPBL)	XP_006714531.1:p.Arg2691Pro
XM_017009329.1:c.*214G>C (NIPBL)	XP_016864818.1:n.*214G>C
XM_017009330.2:c.6653G>C (NIPBL)	XP_016864819.1:p.Arg2218Pro
XM_017009331.1:c.6644G>C (NIPBL)	XP_016864820.1:p.Arg2215Pro
XR_925644.2:n.11935C>G (CPLANE1)
NM_133433.4:c.8270G>C (NIPBL) MANE Select	NP_597677.2:p.Arg2757Pro
NM_015384.5:c.*724G>C (NIPBL)	NP_056199.2:n.*724G>C