Canonical Allele Identifier: CA117056932

Gene: NIPBL

Linked Data

• dbSNP Id: rs759275114
• gnomAD v2: 5-37061061-A-G
• gnomAD v4: 5-37060959-A-G
• MyVariant Identifiers: chr5:g.37061061A>G (hg19) ; chr5:g.37060959A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37060959A>G , CM000667.2:g.37060959A>G	GRCh38
NC_000005.9:g.37061061A>G , CM000667.1:g.37061061A>G	GRCh37
NC_000005.8:g.37096818A>G	NCBI36
NG_006987.1:g.189077A>G
NG_006987.2:g.189077A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7801A>G MANE Select	ENSP00000282516.8:p.Met2601Val
ENST00000652901.1:c.7654A>G	ENSP00000499536.1:p.Met2552Val
ENST00000282516.12:c.7801A>G	ENSP00000282516.8:p.Met2601Val
ENST00000448238.2:c.7801A>G	ENSP00000406266.2:p.Met2601Val
ENST00000513819.1:c.263+1794A>G	ENSP00000421504.1:n.263+1794A>G
ENST00000514335.1:n.1683A>G
ENST00000621733.1:c.1-3619A>G	ENSP00000480694.1:n.1-3619A>G
NM_015384.4:c.7801A>G	NP_056199.2:p.Met2601Val
NM_133433.3:c.7801A>G	NP_597677.2:p.Met2601Val
XM_005248280.2:c.7801A>G	XP_005248337.1:p.Met2601Val
XM_005248282.3:c.7057A>G	XP_005248339.2:p.Met2353Val
XM_006714467.2:c.7654A>G	XP_006714530.1:p.Met2552Val
XM_006714468.1:c.7603A>G	XP_006714531.1:p.Met2535Val
XM_011514014.1:c.7420A>G	XP_011512316.1:p.Met2474Val
XM_005248280.3:c.7801A>G	XP_005248337.1:p.Met2601Val
XM_005248282.5:c.7141A>G	XP_005248339.3:p.Met2381Val
XM_006714468.2:c.7603A>G	XP_006714531.1:p.Met2535Val
XM_017009329.1:c.7654A>G	XP_016864818.1:p.Met2552Val
XM_017009330.2:c.6184A>G	XP_016864819.1:p.Met2062Val
XM_017009331.1:c.6175A>G	XP_016864820.1:p.Met2059Val
NM_133433.4:c.7801A>G MANE Select	NP_597677.2:p.Met2601Val
NM_015384.5:c.7801A>G	NP_056199.2:p.Met2601Val