Canonical Allele Identifier: CA359503957

Gene: NIPBL

Linked Data

• gnomAD v4: 5-37045446-C-T
• MyVariant Identifiers: chr5:g.37045548C>T (hg19) ; chr5:g.37045446C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37045446C>T , CM000667.2:g.37045446C>T	GRCh38
NC_000005.9:g.37045548C>T , CM000667.1:g.37045548C>T	GRCh37
NC_000005.8:g.37081305C>T	NCBI36
NG_006987.1:g.173564C>T
NG_006987.2:g.173564C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.6347C>T MANE Select	ENSP00000282516.8:p.Ala2116Val
ENST00000652901.1:c.6347C>T	ENSP00000499536.1:p.Ala2116Val
ENST00000282516.12:c.6347C>T	ENSP00000282516.8:p.Ala2116Val
ENST00000448238.2:c.6347C>T	ENSP00000406266.2:p.Ala2116Val
ENST00000621733.1:c.1-19132C>T	ENSP00000480694.1:n.1-19132C>T
NM_015384.4:c.6347C>T	NP_056199.2:p.Ala2116Val
NM_133433.3:c.6347C>T	NP_597677.2:p.Ala2116Val
XM_005248280.2:c.6347C>T	XP_005248337.1:p.Ala2116Val
XM_005248282.3:c.5603C>T	XP_005248339.2:p.Ala1868Val
XM_006714467.2:c.6347C>T	XP_006714530.1:p.Ala2116Val
XM_006714468.1:c.6149C>T	XP_006714531.1:p.Ala2050Val
XM_011514014.1:c.5966C>T	XP_011512316.1:p.Ala1989Val
XM_011514015.1:c.6347C>T	XP_011512317.1:p.Ala2116Val
XM_005248280.3:c.6347C>T	XP_005248337.1:p.Ala2116Val
XM_005248282.5:c.5687C>T	XP_005248339.3:p.Ala1896Val
XM_006714468.2:c.6149C>T	XP_006714531.1:p.Ala2050Val
XM_017009329.1:c.6347C>T	XP_016864818.1:p.Ala2116Val
XM_017009330.2:c.4730C>T	XP_016864819.1:p.Ala1577Val
XM_017009331.1:c.4721C>T	XP_016864820.1:p.Ala1574Val
NM_133433.4:c.6347C>T MANE Select	NP_597677.2:p.Ala2116Val
NM_015384.5:c.6347C>T	NP_056199.2:p.Ala2116Val