Canonical Allele Identifier: CA359488453

Gene: NIPBL

Linked Data

• dbSNP Id: rs1202393322
• gnomAD v2: 5-37020966-T-C
• gnomAD v4: 5-37020864-T-C
• MyVariant Identifiers: chr5:g.37020966T>C (hg19) ; chr5:g.37020864T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37020864T>C , CM000667.2:g.37020864T>C	GRCh38
NC_000005.9:g.37020966T>C , CM000667.1:g.37020966T>C	GRCh37
NC_000005.8:g.37056723T>C	NCBI36
NG_006987.1:g.148982T>C
NG_006987.2:g.148982T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5315T>C MANE Select	ENSP00000282516.8:p.Ile1772Thr
ENST00000652901.1:c.5315T>C	ENSP00000499536.1:p.Ile1772Thr
ENST00000282516.12:c.5315T>C	ENSP00000282516.8:p.Ile1772Thr
ENST00000448238.2:c.5315T>C	ENSP00000406266.2:p.Ile1772Thr
ENST00000621733.1:c.1-43714T>C	ENSP00000480694.1:n.1-43714T>C
NM_015384.4:c.5315T>C	NP_056199.2:p.Ile1772Thr
NM_133433.3:c.5315T>C	NP_597677.2:p.Ile1772Thr
XM_005248280.2:c.5315T>C	XP_005248337.1:p.Ile1772Thr
XM_005248282.3:c.4571T>C	XP_005248339.2:p.Ile1524Thr
XM_006714467.2:c.5315T>C	XP_006714530.1:p.Ile1772Thr
XM_006714468.1:c.5117T>C	XP_006714531.1:p.Ile1706Thr
XM_011514014.1:c.4934T>C	XP_011512316.1:p.Ile1645Thr
XM_011514015.1:c.5315T>C	XP_011512317.1:p.Ile1772Thr
XM_005248280.3:c.5315T>C	XP_005248337.1:p.Ile1772Thr
XM_005248282.5:c.4655T>C	XP_005248339.3:p.Ile1552Thr
XM_006714468.2:c.5117T>C	XP_006714531.1:p.Ile1706Thr
XM_017009329.1:c.5315T>C	XP_016864818.1:p.Ile1772Thr
XM_017009330.2:c.3698T>C	XP_016864819.1:p.Ile1233Thr
XM_017009331.1:c.3689T>C	XP_016864820.1:p.Ile1230Thr
NM_133433.4:c.5315T>C MANE Select	NP_597677.2:p.Ile1772Thr
NM_015384.5:c.5315T>C	NP_056199.2:p.Ile1772Thr