Canonical Allele Identifier: CA359519308

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37001151A>T (hg19) ; chr5:g.37001049A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37001049A>T , CM000667.2:g.37001049A>T	GRCh38
NC_000005.9:g.37001151A>T , CM000667.1:g.37001151A>T	GRCh37
NC_000005.8:g.37036908A>T	NCBI36
NG_006987.1:g.129167A>T
NG_006987.2:g.129167A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.3635A>T MANE Select	ENSP00000282516.8:p.Asn1212Ile
ENST00000652901.1:c.3635A>T	ENSP00000499536.1:p.Asn1212Ile
ENST00000282516.12:c.3635A>T	ENSP00000282516.8:p.Asn1212Ile
ENST00000448238.2:c.3635A>T	ENSP00000406266.2:p.Asn1212Ile
ENST00000621733.1:c.1-63529A>T	ENSP00000480694.1:n.1-63529A>T
NM_015384.4:c.3635A>T	NP_056199.2:p.Asn1212Ile
NM_133433.3:c.3635A>T	NP_597677.2:p.Asn1212Ile
XM_005248280.2:c.3635A>T	XP_005248337.1:p.Asn1212Ile
XM_005248282.3:c.2891A>T	XP_005248339.2:p.Asn964Ile
XM_006714467.2:c.3635A>T	XP_006714530.1:p.Asn1212Ile
XM_006714468.1:c.3437A>T	XP_006714531.1:p.Asn1146Ile
XM_011514014.1:c.3254A>T	XP_011512316.1:p.Asn1085Ile
XM_011514015.1:c.3635A>T	XP_011512317.1:p.Asn1212Ile
XM_005248280.3:c.3635A>T	XP_005248337.1:p.Asn1212Ile
XM_005248282.5:c.2975A>T	XP_005248339.3:p.Asn992Ile
XM_006714468.2:c.3437A>T	XP_006714531.1:p.Asn1146Ile
XM_017009329.1:c.3635A>T	XP_016864818.1:p.Asn1212Ile
XM_017009330.2:c.2018A>T	XP_016864819.1:p.Asn673Ile
XM_017009331.1:c.2009A>T	XP_016864820.1:p.Asn670Ile
NM_133433.4:c.3635A>T MANE Select	NP_597677.2:p.Asn1212Ile
NM_015384.5:c.3635A>T	NP_056199.2:p.Asn1212Ile