Canonical Allele Identifier: CA359523832

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064969C>G (hg19) ; chr5:g.37064867C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064867C>G , CM000667.2:g.37064867C>G	GRCh38
NC_000005.9:g.37064969C>G , CM000667.1:g.37064969C>G	GRCh37
NC_000005.8:g.37100726C>G	NCBI36
NG_006987.1:g.192985C>G
NG_006987.2:g.192985C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.8390C>G (NIPBL) MANE Select	ENSP00000282516.8:p.Ala2797Gly
ENST00000652901.1:c.*334C>G (NIPBL)	ENSP00000499536.1:n.*334C>G
ENST00000282516.12:c.8390C>G (NIPBL)	ENSP00000282516.8:p.Ala2797Gly
ENST00000514335.1:n.2313C>G (NIPBL)
ENST00000621733.1:c.290C>G (NIPBL)	ENSP00000480694.1:p.Ala97Gly
NM_015384.4:c.*844C>G (NIPBL)	NP_056199.2:n.*844C>G
NM_133433.3:c.8390C>G (NIPBL)	NP_597677.2:p.Ala2797Gly
XM_005248280.2:c.*334C>G (NIPBL)	XP_005248337.1:n.*334C>G
XM_005248282.3:c.7646C>G (NIPBL)	XP_005248339.2:p.Ala2549Gly
XM_006714467.2:c.8243C>G (NIPBL)	XP_006714530.1:p.Ala2748Gly
XM_006714468.1:c.8192C>G (NIPBL)	XP_006714531.1:p.Ala2731Gly
XM_011514014.1:c.8009C>G (NIPBL)	XP_011512316.1:p.Ala2670Gly
XM_005248280.3:c.*334C>G (NIPBL)	XP_005248337.1:n.*334C>G
XM_005248282.5:c.7730C>G (NIPBL)	XP_005248339.3:p.Ala2577Gly
XM_006714468.2:c.8192C>G (NIPBL)	XP_006714531.1:p.Ala2731Gly
XM_017009329.1:c.*334C>G (NIPBL)	XP_016864818.1:n.*334C>G
XM_017009330.2:c.6773C>G (NIPBL)	XP_016864819.1:p.Ala2258Gly
XM_017009331.1:c.6764C>G (NIPBL)	XP_016864820.1:p.Ala2255Gly
XR_925644.2:n.11815G>C (CPLANE1)
NM_133433.4:c.8390C>G (NIPBL) MANE Select	NP_597677.2:p.Ala2797Gly
NM_015384.5:c.*844C>G (NIPBL)	NP_056199.2:n.*844C>G