Canonical Allele Identifier: CA359500376

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.36985564G>C (hg19) ; chr5:g.36985462G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36985462G>C , CM000667.2:g.36985462G>C	GRCh38
NC_000005.9:g.36985564G>C , CM000667.1:g.36985564G>C	GRCh37
NC_000005.8:g.37021321G>C	NCBI36
NG_006987.1:g.113580G>C
NG_006987.2:g.113580G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.2282G>C MANE Select	ENSP00000282516.8:p.Arg761Thr
ENST00000652901.1:c.2282G>C	ENSP00000499536.1:p.Arg761Thr
ENST00000282516.12:c.2282G>C	ENSP00000282516.8:p.Arg761Thr
ENST00000448238.2:c.2282G>C	ENSP00000406266.2:p.Arg761Thr
ENST00000504430.5:n.1902G>C
ENST00000621733.1:c.1-79116G>C	ENSP00000480694.1:n.1-79116G>C
NM_015384.4:c.2282G>C	NP_056199.2:p.Arg761Thr
NM_133433.3:c.2282G>C	NP_597677.2:p.Arg761Thr
XM_005248280.2:c.2282G>C	XP_005248337.1:p.Arg761Thr
XM_005248282.3:c.1538G>C	XP_005248339.2:p.Arg513Thr
XM_006714467.2:c.2282G>C	XP_006714530.1:p.Arg761Thr
XM_006714468.1:c.2282G>C	XP_006714531.1:p.Arg761Thr
XM_011514014.1:c.2282G>C	XP_011512316.1:p.Arg761Thr
XM_011514015.1:c.2282G>C	XP_011512317.1:p.Arg761Thr
XM_005248280.3:c.2282G>C	XP_005248337.1:p.Arg761Thr
XM_005248282.5:c.1622G>C	XP_005248339.3:p.Arg541Thr
XM_006714468.2:c.2282G>C	XP_006714531.1:p.Arg761Thr
XM_017009329.1:c.2282G>C	XP_016864818.1:p.Arg761Thr
XM_017009330.2:c.665G>C	XP_016864819.1:p.Arg222Thr
XM_017009331.1:c.1495+9060G>C	XP_016864820.1:n.1495+9060G>C
NM_133433.4:c.2282G>C MANE Select	NP_597677.2:p.Arg761Thr
NM_015384.5:c.2282G>C	NP_056199.2:p.Arg761Thr