Canonical Allele Identifier: CA359518400

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37000978C>A (hg19) ; chr5:g.37000876C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37000876C>A , CM000667.2:g.37000876C>A	GRCh38
NC_000005.9:g.37000978C>A , CM000667.1:g.37000978C>A	GRCh37
NC_000005.8:g.37036735C>A	NCBI36
NG_006987.1:g.128994C>A
NG_006987.2:g.128994C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.3562C>A MANE Select	ENSP00000282516.8:p.Leu1188Ile
ENST00000652901.1:c.3562C>A	ENSP00000499536.1:p.Leu1188Ile
ENST00000282516.12:c.3562C>A	ENSP00000282516.8:p.Leu1188Ile
ENST00000448238.2:c.3562C>A	ENSP00000406266.2:p.Leu1188Ile
ENST00000621733.1:c.1-63702C>A	ENSP00000480694.1:n.1-63702C>A
NM_015384.4:c.3562C>A	NP_056199.2:p.Leu1188Ile
NM_133433.3:c.3562C>A	NP_597677.2:p.Leu1188Ile
XM_005248280.2:c.3562C>A	XP_005248337.1:p.Leu1188Ile
XM_005248282.3:c.2818C>A	XP_005248339.2:p.Leu940Ile
XM_006714467.2:c.3562C>A	XP_006714530.1:p.Leu1188Ile
XM_006714468.1:c.3364C>A	XP_006714531.1:p.Leu1122Ile
XM_011514014.1:c.3181C>A	XP_011512316.1:p.Leu1061Ile
XM_011514015.1:c.3562C>A	XP_011512317.1:p.Leu1188Ile
XM_005248280.3:c.3562C>A	XP_005248337.1:p.Leu1188Ile
XM_005248282.5:c.2902C>A	XP_005248339.3:p.Leu968Ile
XM_006714468.2:c.3364C>A	XP_006714531.1:p.Leu1122Ile
XM_017009329.1:c.3562C>A	XP_016864818.1:p.Leu1188Ile
XM_017009330.2:c.1945C>A	XP_016864819.1:p.Leu649Ile
XM_017009331.1:c.1936C>A	XP_016864820.1:p.Leu646Ile
NM_133433.4:c.3562C>A MANE Select	NP_597677.2:p.Leu1188Ile
NM_015384.5:c.3562C>A	NP_056199.2:p.Leu1188Ile