Canonical Allele Identifier: CA359518080

Gene: NIPBL

Linked Data

• COSMIC: COSM6020200 ; COSM6020201
• MyVariant Identifiers: chr5:g.37000935G>C (hg19) ; chr5:g.37000833G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37000833G>C , CM000667.2:g.37000833G>C	GRCh38
NC_000005.9:g.37000935G>C , CM000667.1:g.37000935G>C	GRCh37
NC_000005.8:g.37036692G>C	NCBI36
NG_006987.1:g.128951G>C
NG_006987.2:g.128951G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.3519G>C MANE Select	ENSP00000282516.8:p.Lys1173Asn
ENST00000652901.1:c.3519G>C	ENSP00000499536.1:p.Lys1173Asn
ENST00000282516.12:c.3519G>C	ENSP00000282516.8:p.Lys1173Asn
ENST00000448238.2:c.3519G>C	ENSP00000406266.2:p.Lys1173Asn
ENST00000621733.1:c.1-63745G>C	ENSP00000480694.1:n.1-63745G>C
NM_015384.4:c.3519G>C	NP_056199.2:p.Lys1173Asn
NM_133433.3:c.3519G>C	NP_597677.2:p.Lys1173Asn
XM_005248280.2:c.3519G>C	XP_005248337.1:p.Lys1173Asn
XM_005248282.3:c.2775G>C	XP_005248339.2:p.Lys925Asn
XM_006714467.2:c.3519G>C	XP_006714530.1:p.Lys1173Asn
XM_006714468.1:c.3321G>C	XP_006714531.1:p.Lys1107Asn
XM_011514014.1:c.3138G>C	XP_011512316.1:p.Lys1046Asn
XM_011514015.1:c.3519G>C	XP_011512317.1:p.Lys1173Asn
XM_005248280.3:c.3519G>C	XP_005248337.1:p.Lys1173Asn
XM_005248282.5:c.2859G>C	XP_005248339.3:p.Lys953Asn
XM_006714468.2:c.3321G>C	XP_006714531.1:p.Lys1107Asn
XM_017009329.1:c.3519G>C	XP_016864818.1:p.Lys1173Asn
XM_017009330.2:c.1902G>C	XP_016864819.1:p.Lys634Asn
XM_017009331.1:c.1893G>C	XP_016864820.1:p.Lys631Asn
NM_133433.4:c.3519G>C MANE Select	NP_597677.2:p.Lys1173Asn
NM_015384.5:c.3519G>C	NP_056199.2:p.Lys1173Asn