Canonical Allele Identifier: CA359522365

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064740C>G (hg19) ; chr5:g.37064638C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064638C>G , CM000667.2:g.37064638C>G	GRCh38
NC_000005.9:g.37064740C>G , CM000667.1:g.37064740C>G	GRCh37
NC_000005.8:g.37100497C>G	NCBI36
NG_006987.1:g.192756C>G
NG_006987.2:g.192756C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8161C>G (NIPBL) MANE Select	ENSP00000282516.8:p.Arg2721Gly
ENST00000652901.1:c.*105C>G (NIPBL)	ENSP00000499536.1:n.*105C>G
ENST00000282516.12:c.8161C>G (NIPBL)	ENSP00000282516.8:p.Arg2721Gly
ENST00000514335.1:n.2084C>G (NIPBL)
ENST00000621733.1:c.61C>G (NIPBL)	ENSP00000480694.1:p.Arg21Gly
NM_015384.4:c.*615C>G (NIPBL)	NP_056199.2:n.*615C>G
NM_133433.3:c.8161C>G (NIPBL)	NP_597677.2:p.Arg2721Gly
XM_005248280.2:c.*105C>G (NIPBL)	XP_005248337.1:n.*105C>G
XM_005248282.3:c.7417C>G (NIPBL)	XP_005248339.2:p.Arg2473Gly
XM_006714467.2:c.8014C>G (NIPBL)	XP_006714530.1:p.Arg2672Gly
XM_006714468.1:c.7963C>G (NIPBL)	XP_006714531.1:p.Arg2655Gly
XM_011514014.1:c.7780C>G (NIPBL)	XP_011512316.1:p.Arg2594Gly
XM_005248280.3:c.*105C>G (NIPBL)	XP_005248337.1:n.*105C>G
XM_005248282.5:c.7501C>G (NIPBL)	XP_005248339.3:p.Arg2501Gly
XM_006714468.2:c.7963C>G (NIPBL)	XP_006714531.1:p.Arg2655Gly
XM_017009329.1:c.*105C>G (NIPBL)	XP_016864818.1:n.*105C>G
XM_017009330.2:c.6544C>G (NIPBL)	XP_016864819.1:p.Arg2182Gly
XM_017009331.1:c.6535C>G (NIPBL)	XP_016864820.1:p.Arg2179Gly
XR_925644.2:n.12044G>C (CPLANE1)
NM_133433.4:c.8161C>G (NIPBL) MANE Select	NP_597677.2:p.Arg2721Gly
NM_015384.5:c.*615C>G (NIPBL)	NP_056199.2:n.*615C>G