Canonical Allele Identifier: CA359505083

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37045698A>C (hg19) ; chr5:g.37045596A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37045596A>C , CM000667.2:g.37045596A>C	GRCh38
NC_000005.9:g.37045698A>C , CM000667.1:g.37045698A>C	GRCh37
NC_000005.8:g.37081455A>C	NCBI36
NG_006987.1:g.173714A>C
NG_006987.2:g.173714A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.6497A>C MANE Select	ENSP00000282516.8:p.Lys2166Thr
ENST00000652901.1:c.6497A>C	ENSP00000499536.1:p.Lys2166Thr
ENST00000282516.12:c.6497A>C	ENSP00000282516.8:p.Lys2166Thr
ENST00000448238.2:c.6497A>C	ENSP00000406266.2:p.Lys2166Thr
ENST00000621733.1:c.1-18982A>C	ENSP00000480694.1:n.1-18982A>C
NM_015384.4:c.6497A>C	NP_056199.2:p.Lys2166Thr
NM_133433.3:c.6497A>C	NP_597677.2:p.Lys2166Thr
XM_005248280.2:c.6497A>C	XP_005248337.1:p.Lys2166Thr
XM_005248282.3:c.5753A>C	XP_005248339.2:p.Lys1918Thr
XM_006714467.2:c.6497A>C	XP_006714530.1:p.Lys2166Thr
XM_006714468.1:c.6299A>C	XP_006714531.1:p.Lys2100Thr
XM_011514014.1:c.6116A>C	XP_011512316.1:p.Lys2039Thr
XM_011514015.1:c.6497A>C	XP_011512317.1:p.Lys2166Thr
XM_005248280.3:c.6497A>C	XP_005248337.1:p.Lys2166Thr
XM_005248282.5:c.5837A>C	XP_005248339.3:p.Lys1946Thr
XM_006714468.2:c.6299A>C	XP_006714531.1:p.Lys2100Thr
XM_017009329.1:c.6497A>C	XP_016864818.1:p.Lys2166Thr
XM_017009330.2:c.4880A>C	XP_016864819.1:p.Lys1627Thr
XM_017009331.1:c.4871A>C	XP_016864820.1:p.Lys1624Thr
NM_133433.4:c.6497A>C MANE Select	NP_597677.2:p.Lys2166Thr
NM_015384.5:c.6497A>C	NP_056199.2:p.Lys2166Thr