Canonical Allele Identifier: CA359483044

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37016255T>A (hg19) ; chr5:g.37016153T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37016153T>A , CM000667.2:g.37016153T>A	GRCh38
NC_000005.9:g.37016255T>A , CM000667.1:g.37016255T>A	GRCh37
NC_000005.8:g.37052012T>A	NCBI36
NG_006987.1:g.144271T>A
NG_006987.2:g.144271T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.4759T>A MANE Select	ENSP00000282516.8:p.Leu1587Met
ENST00000652901.1:c.4759T>A	ENSP00000499536.1:p.Leu1587Met
ENST00000282516.12:c.4759T>A	ENSP00000282516.8:p.Leu1587Met
ENST00000448238.2:c.4759T>A	ENSP00000406266.2:p.Leu1587Met
ENST00000621733.1:c.1-48425T>A	ENSP00000480694.1:n.1-48425T>A
NM_015384.4:c.4759T>A	NP_056199.2:p.Leu1587Met
NM_133433.3:c.4759T>A	NP_597677.2:p.Leu1587Met
XM_005248280.2:c.4759T>A	XP_005248337.1:p.Leu1587Met
XM_005248282.3:c.4015T>A	XP_005248339.2:p.Leu1339Met
XM_006714467.2:c.4759T>A	XP_006714530.1:p.Leu1587Met
XM_006714468.1:c.4561T>A	XP_006714531.1:p.Leu1521Met
XM_011514014.1:c.4378T>A	XP_011512316.1:p.Leu1460Met
XM_011514015.1:c.4759T>A	XP_011512317.1:p.Leu1587Met
XM_005248280.3:c.4759T>A	XP_005248337.1:p.Leu1587Met
XM_005248282.5:c.4099T>A	XP_005248339.3:p.Leu1367Met
XM_006714468.2:c.4561T>A	XP_006714531.1:p.Leu1521Met
XM_017009329.1:c.4759T>A	XP_016864818.1:p.Leu1587Met
XM_017009330.2:c.3142T>A	XP_016864819.1:p.Leu1048Met
XM_017009331.1:c.3133T>A	XP_016864820.1:p.Leu1045Met
NM_133433.4:c.4759T>A MANE Select	NP_597677.2:p.Leu1587Met
NM_015384.5:c.4759T>A	NP_056199.2:p.Leu1587Met