Canonical Allele Identifier: CA359514227

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.36995883A>T (hg19) ; chr5:g.36995781A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.36995781A>T , CM000667.2:g.36995781A>T	GRCh38
NC_000005.9:g.36995883A>T , CM000667.1:g.36995883A>T	GRCh37
NC_000005.8:g.37031640A>T	NCBI36
NG_006987.1:g.123899A>T
NG_006987.2:g.123899A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.3281A>T MANE Select	ENSP00000282516.8:p.Asn1094Ile
ENST00000652901.1:c.3281A>T	ENSP00000499536.1:p.Asn1094Ile
ENST00000282516.12:c.3281A>T	ENSP00000282516.8:p.Asn1094Ile
ENST00000448238.2:c.3281A>T	ENSP00000406266.2:p.Asn1094Ile
ENST00000503274.1:n.632A>T
ENST00000504430.5:n.2901A>T
ENST00000509429.1:n.32A>T
ENST00000621733.1:c.1-68797A>T	ENSP00000480694.1:n.1-68797A>T
NM_015384.4:c.3281A>T	NP_056199.2:p.Asn1094Ile
NM_133433.3:c.3281A>T	NP_597677.2:p.Asn1094Ile
XM_005248280.2:c.3281A>T	XP_005248337.1:p.Asn1094Ile
XM_005248282.3:c.2537A>T	XP_005248339.2:p.Asn846Ile
XM_006714467.2:c.3281A>T	XP_006714530.1:p.Asn1094Ile
XM_006714468.1:c.3281A>T	XP_006714531.1:p.Asn1094Ile
XM_011514014.1:c.3122-5036A>T	XP_011512316.1:n.3122-5036A>T
XM_011514015.1:c.3281A>T	XP_011512317.1:p.Asn1094Ile
XM_005248280.3:c.3281A>T	XP_005248337.1:p.Asn1094Ile
XM_005248282.5:c.2621A>T	XP_005248339.3:p.Asn874Ile
XM_006714468.2:c.3281A>T	XP_006714531.1:p.Asn1094Ile
XM_017009329.1:c.3281A>T	XP_016864818.1:p.Asn1094Ile
XM_017009330.2:c.1664A>T	XP_016864819.1:p.Asn555Ile
XM_017009331.1:c.1655A>T	XP_016864820.1:p.Asn552Ile
NM_133433.4:c.3281A>T MANE Select	NP_597677.2:p.Asn1094Ile
NM_015384.5:c.3281A>T	NP_056199.2:p.Asn1094Ile