Canonical Allele Identifier: CA359509398

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37051879A>T (hg19) ; chr5:g.37051777A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37051777A>T , CM000667.2:g.37051777A>T	GRCh38
NC_000005.9:g.37051879A>T , CM000667.1:g.37051879A>T	GRCh37
NC_000005.8:g.37087636A>T	NCBI36
NG_006987.1:g.179895A>T
NG_006987.2:g.179895A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.6955-2A>T MANE Select	ENSP00000282516.8:n.6955-2A>T
ENST00000652901.1:c.6955-2A>T	ENSP00000499536.1:n.6955-2A>T
ENST00000282516.12:c.6955-2A>T	ENSP00000282516.8:n.6955-2A>T
ENST00000448238.2:c.6955-2A>T	ENSP00000406266.2:n.6955-2A>T
ENST00000514335.1:n.835A>T
ENST00000621733.1:c.1-12801A>T	ENSP00000480694.1:n.1-12801A>T
NM_015384.4:c.6955-2A>T	NP_056199.2:n.6955-2A>T
NM_133433.3:c.6955-2A>T	NP_597677.2:n.6955-2A>T
XM_005248280.2:c.6955-2A>T	XP_005248337.1:n.6955-2A>T
XM_005248282.3:c.6211-2A>T	XP_005248339.2:n.6211-2A>T
XM_006714467.2:c.6955-2A>T	XP_006714530.1:n.6955-2A>T
XM_006714468.1:c.6757-2A>T	XP_006714531.1:n.6757-2A>T
XM_011514014.1:c.6574-2A>T	XP_011512316.1:n.6574-2A>T
XM_011514015.1:c.6955-2A>T	XP_011512317.1:n.6955-2A>T
XM_005248280.3:c.6955-2A>T	XP_005248337.1:n.6955-2A>T
XM_005248282.5:c.6295-2A>T	XP_005248339.3:n.6295-2A>T
XM_006714468.2:c.6757-2A>T	XP_006714531.1:n.6757-2A>T
XM_017009329.1:c.6955-2A>T	XP_016864818.1:n.6955-2A>T
XM_017009330.2:c.5338-2A>T	XP_016864819.1:n.5338-2A>T
XM_017009331.1:c.5329-2A>T	XP_016864820.1:n.5329-2A>T
NM_133433.4:c.6955-2A>T MANE Select	NP_597677.2:n.6955-2A>T
NM_015384.5:c.6955-2A>T	NP_056199.2:n.6955-2A>T