Canonical Allele Identifier: CA359509139

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37049399T>C (hg19) ; chr5:g.37049297T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37049297T>C , CM000667.2:g.37049297T>C	GRCh38
NC_000005.9:g.37049399T>C , CM000667.1:g.37049399T>C	GRCh37
NC_000005.8:g.37085156T>C	NCBI36
NG_006987.1:g.177415T>C
NG_006987.2:g.177415T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.6950T>C MANE Select	ENSP00000282516.8:p.Val2317Ala
ENST00000652901.1:c.6950T>C	ENSP00000499536.1:p.Val2317Ala
ENST00000282516.12:c.6950T>C	ENSP00000282516.8:p.Val2317Ala
ENST00000448238.2:c.6950T>C	ENSP00000406266.2:p.Val2317Ala
ENST00000621733.1:c.1-15281T>C	ENSP00000480694.1:n.1-15281T>C
NM_015384.4:c.6950T>C	NP_056199.2:p.Val2317Ala
NM_133433.3:c.6950T>C	NP_597677.2:p.Val2317Ala
XM_005248280.2:c.6950T>C	XP_005248337.1:p.Val2317Ala
XM_005248282.3:c.6206T>C	XP_005248339.2:p.Val2069Ala
XM_006714467.2:c.6950T>C	XP_006714530.1:p.Val2317Ala
XM_006714468.1:c.6752T>C	XP_006714531.1:p.Val2251Ala
XM_011514014.1:c.6569T>C	XP_011512316.1:p.Val2190Ala
XM_011514015.1:c.6950T>C	XP_011512317.1:p.Val2317Ala
XM_005248280.3:c.6950T>C	XP_005248337.1:p.Val2317Ala
XM_005248282.5:c.6290T>C	XP_005248339.3:p.Val2097Ala
XM_006714468.2:c.6752T>C	XP_006714531.1:p.Val2251Ala
XM_017009329.1:c.6950T>C	XP_016864818.1:p.Val2317Ala
XM_017009330.2:c.5333T>C	XP_016864819.1:p.Val1778Ala
XM_017009331.1:c.5324T>C	XP_016864820.1:p.Val1775Ala
NM_133433.4:c.6950T>C MANE Select	NP_597677.2:p.Val2317Ala
NM_015384.5:c.6950T>C	NP_056199.2:p.Val2317Ala