Canonical Allele Identifier: CA359521991

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064672C>G (hg19) ; chr5:g.37064570C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064570C>G , CM000667.2:g.37064570C>G	GRCh38
NC_000005.9:g.37064672C>G , CM000667.1:g.37064672C>G	GRCh37
NC_000005.8:g.37100429C>G	NCBI36
NG_006987.1:g.192688C>G
NG_006987.2:g.192688C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8093C>G (NIPBL) MANE Select	ENSP00000282516.8:p.Ala2698Gly
ENST00000652901.1:c.*37C>G (NIPBL)	ENSP00000499536.1:n.*37C>G
ENST00000282516.12:c.8093C>G (NIPBL)	ENSP00000282516.8:p.Ala2698Gly
ENST00000514335.1:n.2016C>G (NIPBL)
ENST00000621733.1:c.1-8C>G (NIPBL)	ENSP00000480694.1:n.1-8C>G
NM_015384.4:c.*547C>G (NIPBL)	NP_056199.2:n.*547C>G
NM_133433.3:c.8093C>G (NIPBL)	NP_597677.2:p.Ala2698Gly
XM_005248280.2:c.*37C>G (NIPBL)	XP_005248337.1:n.*37C>G
XM_005248282.3:c.7349C>G (NIPBL)	XP_005248339.2:p.Ala2450Gly
XM_006714467.2:c.7946C>G (NIPBL)	XP_006714530.1:p.Ala2649Gly
XM_006714468.1:c.7895C>G (NIPBL)	XP_006714531.1:p.Ala2632Gly
XM_011514014.1:c.7712C>G (NIPBL)	XP_011512316.1:p.Ala2571Gly
XM_005248280.3:c.*37C>G (NIPBL)	XP_005248337.1:n.*37C>G
XM_005248282.5:c.7433C>G (NIPBL)	XP_005248339.3:p.Ala2478Gly
XM_006714468.2:c.7895C>G (NIPBL)	XP_006714531.1:p.Ala2632Gly
XM_017009329.1:c.*37C>G (NIPBL)	XP_016864818.1:n.*37C>G
XM_017009330.2:c.6476C>G (NIPBL)	XP_016864819.1:p.Ala2159Gly
XM_017009331.1:c.6467C>G (NIPBL)	XP_016864820.1:p.Ala2156Gly
XR_925644.2:n.12112G>C (CPLANE1)
NM_133433.4:c.8093C>G (NIPBL) MANE Select	NP_597677.2:p.Ala2698Gly
NM_015384.5:c.*547C>G (NIPBL)	NP_056199.2:n.*547C>G