Canonical Allele Identifier: CA2673550937

Gene: NIPBL

Linked Data

• gnomAD v4: 5-37003222-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37003222T>C , CM000667.2:g.37003222T>C	GRCh38
NC_000005.9:g.37003324T>C , CM000667.1:g.37003324T>C	GRCh37
NC_000005.8:g.37039081T>C	NCBI36
NG_006987.1:g.131340T>C
NG_006987.2:g.131340T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.3769-39T>C MANE Select	ENSP00000282516.8:n.3769-39T>C
ENST00000652901.1:c.3769-39T>C	ENSP00000499536.1:n.3769-39T>C
ENST00000282516.12:c.3769-39T>C	ENSP00000282516.8:n.3769-39T>C
ENST00000448238.2:c.3769-39T>C	ENSP00000406266.2:n.3769-39T>C
ENST00000621733.1:c.1-61356T>C	ENSP00000480694.1:n.1-61356T>C
NM_015384.4:c.3769-39T>C	NP_056199.2:n.3769-39T>C
NM_133433.3:c.3769-39T>C	NP_597677.2:n.3769-39T>C
XM_005248280.2:c.3769-39T>C	XP_005248337.1:n.3769-39T>C
XM_005248282.3:c.3025-39T>C	XP_005248339.2:n.3025-39T>C
XM_006714467.2:c.3769-39T>C	XP_006714530.1:n.3769-39T>C
XM_006714468.1:c.3571-39T>C	XP_006714531.1:n.3571-39T>C
XM_011514014.1:c.3388-39T>C	XP_011512316.1:n.3388-39T>C
XM_011514015.1:c.3769-39T>C	XP_011512317.1:n.3769-39T>C
XM_005248280.3:c.3769-39T>C	XP_005248337.1:n.3769-39T>C
XM_005248282.5:c.3109-39T>C	XP_005248339.3:n.3109-39T>C
XM_006714468.2:c.3571-39T>C	XP_006714531.1:n.3571-39T>C
XM_017009329.1:c.3769-39T>C	XP_016864818.1:n.3769-39T>C
XM_017009330.2:c.2152-39T>C	XP_016864819.1:n.2152-39T>C
XM_017009331.1:c.2143-39T>C	XP_016864820.1:n.2143-39T>C
NM_133433.4:c.3769-39T>C MANE Select	NP_597677.2:n.3769-39T>C
NM_015384.5:c.3769-39T>C	NP_056199.2:n.3769-39T>C