Canonical Allele Identifier: CA359521739

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064632T>A (hg19) ; chr5:g.37064530T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064530T>A , CM000667.2:g.37064530T>A	GRCh38
NC_000005.9:g.37064632T>A , CM000667.1:g.37064632T>A	GRCh37
NC_000005.8:g.37100389T>A	NCBI36
NG_006987.1:g.192648T>A
NG_006987.2:g.192648T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8053T>A (NIPBL) MANE Select	ENSP00000282516.8:p.Leu2685Met
ENST00000652901.1:c.7947T>A (NIPBL)	ENSP00000499536.1:p.His2649Gln
ENST00000282516.12:c.8053T>A (NIPBL)	ENSP00000282516.8:p.Leu2685Met
ENST00000514335.1:n.1976T>A (NIPBL)
ENST00000621733.1:c.1-48T>A (NIPBL)	ENSP00000480694.1:n.1-48T>A
NM_015384.4:c.*507T>A (NIPBL)	NP_056199.2:n.*507T>A
NM_133433.3:c.8053T>A (NIPBL)	NP_597677.2:p.Leu2685Met
XM_005248280.2:c.8094T>A (NIPBL)	XP_005248337.1:p.His2698Gln
XM_005248282.3:c.7309T>A (NIPBL)	XP_005248339.2:p.Leu2437Met
XM_006714467.2:c.7906T>A (NIPBL)	XP_006714530.1:p.Leu2636Met
XM_006714468.1:c.7855T>A (NIPBL)	XP_006714531.1:p.Leu2619Met
XM_011514014.1:c.7672T>A (NIPBL)	XP_011512316.1:p.Leu2558Met
XM_005248280.3:c.8094T>A (NIPBL)	XP_005248337.1:p.His2698Gln
XM_005248282.5:c.7393T>A (NIPBL)	XP_005248339.3:p.Leu2465Met
XM_006714468.2:c.7855T>A (NIPBL)	XP_006714531.1:p.Leu2619Met
XM_017009329.1:c.7947T>A (NIPBL)	XP_016864818.1:p.His2649Gln
XM_017009330.2:c.6436T>A (NIPBL)	XP_016864819.1:p.Leu2146Met
XM_017009331.1:c.6427T>A (NIPBL)	XP_016864820.1:p.Leu2143Met
XR_925644.2:n.12152A>T (CPLANE1)
NM_133433.4:c.8053T>A (NIPBL) MANE Select	NP_597677.2:p.Leu2685Met
NM_015384.5:c.*507T>A (NIPBL)	NP_056199.2:n.*507T>A