Canonical Allele Identifier: CA359488503

Gene: NIPBL

Linked Data

• gnomAD v4: 5-37020871-G-T
• MyVariant Identifiers: chr5:g.37020973G>T (hg19) ; chr5:g.37020871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37020871G>T , CM000667.2:g.37020871G>T	GRCh38
NC_000005.9:g.37020973G>T , CM000667.1:g.37020973G>T	GRCh37
NC_000005.8:g.37056730G>T	NCBI36
NG_006987.1:g.148989G>T
NG_006987.2:g.148989G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.5322G>T MANE Select	ENSP00000282516.8:p.Leu1774Phe
ENST00000652901.1:c.5322G>T	ENSP00000499536.1:p.Leu1774Phe
ENST00000282516.12:c.5322G>T	ENSP00000282516.8:p.Leu1774Phe
ENST00000448238.2:c.5322G>T	ENSP00000406266.2:p.Leu1774Phe
ENST00000621733.1:c.1-43707G>T	ENSP00000480694.1:n.1-43707G>T
NM_015384.4:c.5322G>T	NP_056199.2:p.Leu1774Phe
NM_133433.3:c.5322G>T	NP_597677.2:p.Leu1774Phe
XM_005248280.2:c.5322G>T	XP_005248337.1:p.Leu1774Phe
XM_005248282.3:c.4578G>T	XP_005248339.2:p.Leu1526Phe
XM_006714467.2:c.5322G>T	XP_006714530.1:p.Leu1774Phe
XM_006714468.1:c.5124G>T	XP_006714531.1:p.Leu1708Phe
XM_011514014.1:c.4941G>T	XP_011512316.1:p.Leu1647Phe
XM_011514015.1:c.5322G>T	XP_011512317.1:p.Leu1774Phe
XM_005248280.3:c.5322G>T	XP_005248337.1:p.Leu1774Phe
XM_005248282.5:c.4662G>T	XP_005248339.3:p.Leu1554Phe
XM_006714468.2:c.5124G>T	XP_006714531.1:p.Leu1708Phe
XM_017009329.1:c.5322G>T	XP_016864818.1:p.Leu1774Phe
XM_017009330.2:c.3705G>T	XP_016864819.1:p.Leu1235Phe
XM_017009331.1:c.3696G>T	XP_016864820.1:p.Leu1232Phe
NM_133433.4:c.5322G>T MANE Select	NP_597677.2:p.Leu1774Phe
NM_015384.5:c.5322G>T	NP_056199.2:p.Leu1774Phe