Canonical Allele Identifier: CA443912038

Gene: NIPBL

Linked Data

• dbSNP Id: rs1579583711
• MyVariant Identifiers: chr5:g.37052626A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37052524A>C , CM000667.2:g.37052524A>C	GRCh38
NC_000005.9:g.37052626A>C , CM000667.1:g.37052626A>C	GRCh37
NC_000005.8:g.37088383A>C	NCBI36
NG_006987.1:g.180642A>C
NG_006987.2:g.180642A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000282516.13:c.7221A>C MANE Select	ENSP00000282516.8:p.Arg2407=
ENST00000652901.1:c.7221A>C	ENSP00000499536.1:p.Arg2407=
ENST00000282516.12:c.7221A>C	ENSP00000282516.8:p.Arg2407=
ENST00000448238.2:c.7221A>C	ENSP00000406266.2:p.Arg2407=
ENST00000514335.1:n.1103A>C
ENST00000621733.1:c.1-12054A>C	ENSP00000480694.1:n.1-12054A>C
NM_015384.4:c.7221A>C	NP_056199.2:p.Arg2407=
NM_133433.3:c.7221A>C	NP_597677.2:p.Arg2407=
XM_005248280.2:c.7221A>C	XP_005248337.1:p.Arg2407=
XM_005248282.3:c.6477A>C	XP_005248339.2:p.Arg2159=
XM_006714467.2:c.7221A>C	XP_006714530.1:p.Arg2407=
XM_006714468.1:c.7023A>C	XP_006714531.1:p.Arg2341=
XM_011514014.1:c.6840A>C	XP_011512316.1:p.Arg2280=
XM_011514015.1:c.7221A>C	XP_011512317.1:p.Arg2407=
XM_005248280.3:c.7221A>C	XP_005248337.1:p.Arg2407=
XM_005248282.5:c.6561A>C	XP_005248339.3:p.Arg2187=
XM_006714468.2:c.7023A>C	XP_006714531.1:p.Arg2341=
XM_017009329.1:c.7221A>C	XP_016864818.1:p.Arg2407=
XM_017009330.2:c.5604A>C	XP_016864819.1:p.Arg1868=
XM_017009331.1:c.5595A>C	XP_016864820.1:p.Arg1865=
NM_133433.4:c.7221A>C MANE Select	NP_597677.2:p.Arg2407=
NM_015384.5:c.7221A>C	NP_056199.2:p.Arg2407=