Canonical Allele Identifier: CA359522596

Gene: NIPBL CPLANE1

Linked Data

• MyVariant Identifiers: chr5:g.37064799G>C (hg19) ; chr5:g.37064697G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37064697G>C , CM000667.2:g.37064697G>C	GRCh38
NC_000005.9:g.37064799G>C , CM000667.1:g.37064799G>C	GRCh37
NC_000005.8:g.37100556G>C	NCBI36
NG_006987.1:g.192815G>C
NG_006987.2:g.192815G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.8220G>C (NIPBL) MANE Select	ENSP00000282516.8:p.Met2740Ile
ENST00000652901.1:c.*164G>C (NIPBL)	ENSP00000499536.1:n.*164G>C
ENST00000282516.12:c.8220G>C (NIPBL)	ENSP00000282516.8:p.Met2740Ile
ENST00000514335.1:n.2143G>C (NIPBL)
ENST00000621733.1:c.120G>C (NIPBL)	ENSP00000480694.1:p.Met40Ile
NM_015384.4:c.*674G>C (NIPBL)	NP_056199.2:n.*674G>C
NM_133433.3:c.8220G>C (NIPBL)	NP_597677.2:p.Met2740Ile
XM_005248280.2:c.*164G>C (NIPBL)	XP_005248337.1:n.*164G>C
XM_005248282.3:c.7476G>C (NIPBL)	XP_005248339.2:p.Met2492Ile
XM_006714467.2:c.8073G>C (NIPBL)	XP_006714530.1:p.Met2691Ile
XM_006714468.1:c.8022G>C (NIPBL)	XP_006714531.1:p.Met2674Ile
XM_011514014.1:c.7839G>C (NIPBL)	XP_011512316.1:p.Met2613Ile
XM_005248280.3:c.*164G>C (NIPBL)	XP_005248337.1:n.*164G>C
XM_005248282.5:c.7560G>C (NIPBL)	XP_005248339.3:p.Met2520Ile
XM_006714468.2:c.8022G>C (NIPBL)	XP_006714531.1:p.Met2674Ile
XM_017009329.1:c.*164G>C (NIPBL)	XP_016864818.1:n.*164G>C
XM_017009330.2:c.6603G>C (NIPBL)	XP_016864819.1:p.Met2201Ile
XM_017009331.1:c.6594G>C (NIPBL)	XP_016864820.1:p.Met2198Ile
XR_925644.2:n.11985C>G (CPLANE1)
NM_133433.4:c.8220G>C (NIPBL) MANE Select	NP_597677.2:p.Met2740Ile
NM_015384.5:c.*674G>C (NIPBL)	NP_056199.2:n.*674G>C