Canonical Allele Identifier: CA443905741

Gene: NIPBL

Linked Data

• dbSNP Id: rs1389928995
• gnomAD v4: 5-37036448-C-T
• MyVariant Identifiers: chr5:g.37036550C>T (hg19) ; chr5:g.37036448C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37036448C>T , CM000667.2:g.37036448C>T	GRCh38
NC_000005.9:g.37036550C>T , CM000667.1:g.37036550C>T	GRCh37
NC_000005.8:g.37072307C>T	NCBI36
NG_006987.1:g.164566C>T
NG_006987.2:g.164566C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5932C>T MANE Select	ENSP00000282516.8:p.Leu1978=
ENST00000652901.1:c.5932C>T	ENSP00000499536.1:p.Leu1978=
ENST00000282516.12:c.5932C>T	ENSP00000282516.8:p.Leu1978=
ENST00000448238.2:c.5932C>T	ENSP00000406266.2:p.Leu1978=
ENST00000621733.1:c.1-28130C>T	ENSP00000480694.1:n.1-28130C>T
NM_015384.4:c.5932C>T	NP_056199.2:p.Leu1978=
NM_133433.3:c.5932C>T	NP_597677.2:p.Leu1978=
XM_005248280.2:c.5932C>T	XP_005248337.1:p.Leu1978=
XM_005248282.3:c.5188C>T	XP_005248339.2:p.Leu1730=
XM_006714467.2:c.5932C>T	XP_006714530.1:p.Leu1978=
XM_006714468.1:c.5734C>T	XP_006714531.1:p.Leu1912=
XM_011514014.1:c.5551C>T	XP_011512316.1:p.Leu1851=
XM_011514015.1:c.5932C>T	XP_011512317.1:p.Leu1978=
XM_005248280.3:c.5932C>T	XP_005248337.1:p.Leu1978=
XM_005248282.5:c.5272C>T	XP_005248339.3:p.Leu1758=
XM_006714468.2:c.5734C>T	XP_006714531.1:p.Leu1912=
XM_017009329.1:c.5932C>T	XP_016864818.1:p.Leu1978=
XM_017009330.2:c.4315C>T	XP_016864819.1:p.Leu1439=
XM_017009331.1:c.4306C>T	XP_016864820.1:p.Leu1436=
NM_133433.4:c.5932C>T MANE Select	NP_597677.2:p.Leu1978=
NM_015384.5:c.5932C>T	NP_056199.2:p.Leu1978=