Canonical Allele Identifier: CA443905086

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37020728T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37020626T>C , CM000667.2:g.37020626T>C	GRCh38
NC_000005.9:g.37020728T>C , CM000667.1:g.37020728T>C	GRCh37
NC_000005.8:g.37056485T>C	NCBI36
NG_006987.1:g.148744T>C
NG_006987.2:g.148744T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.5178T>C MANE Select	ENSP00000282516.8:p.Phe1726=
ENST00000652901.1:c.5178T>C	ENSP00000499536.1:p.Phe1726=
ENST00000282516.12:c.5178T>C	ENSP00000282516.8:p.Phe1726=
ENST00000448238.2:c.5178T>C	ENSP00000406266.2:p.Phe1726=
ENST00000621733.1:c.1-43952T>C	ENSP00000480694.1:n.1-43952T>C
NM_015384.4:c.5178T>C	NP_056199.2:p.Phe1726=
NM_133433.3:c.5178T>C	NP_597677.2:p.Phe1726=
XM_005248280.2:c.5178T>C	XP_005248337.1:p.Phe1726=
XM_005248282.3:c.4434T>C	XP_005248339.2:p.Phe1478=
XM_006714467.2:c.5178T>C	XP_006714530.1:p.Phe1726=
XM_006714468.1:c.4980T>C	XP_006714531.1:p.Phe1660=
XM_011514014.1:c.4797T>C	XP_011512316.1:p.Phe1599=
XM_011514015.1:c.5178T>C	XP_011512317.1:p.Phe1726=
XM_005248280.3:c.5178T>C	XP_005248337.1:p.Phe1726=
XM_005248282.5:c.4518T>C	XP_005248339.3:p.Phe1506=
XM_006714468.2:c.4980T>C	XP_006714531.1:p.Phe1660=
XM_017009329.1:c.5178T>C	XP_016864818.1:p.Phe1726=
XM_017009330.2:c.3561T>C	XP_016864819.1:p.Phe1187=
XM_017009331.1:c.3552T>C	XP_016864820.1:p.Phe1184=
NM_133433.4:c.5178T>C MANE Select	NP_597677.2:p.Phe1726=
NM_015384.5:c.5178T>C	NP_056199.2:p.Phe1726=