Canonical Allele Identifier: CA359518214

Gene: NIPBL

Linked Data

• MyVariant Identifiers: chr5:g.37060952T>G (hg19) ; chr5:g.37060850T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37060850T>G , CM000667.2:g.37060850T>G	GRCh38
NC_000005.9:g.37060952T>G , CM000667.1:g.37060952T>G	GRCh37
NC_000005.8:g.37096709T>G	NCBI36
NG_006987.1:g.188968T>G
NG_006987.2:g.188968T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.7692T>G MANE Select	ENSP00000282516.8:p.Ile2564Met
ENST00000652901.1:c.7545T>G	ENSP00000499536.1:p.Ile2515Met
ENST00000282516.12:c.7692T>G	ENSP00000282516.8:p.Ile2564Met
ENST00000448238.2:c.7692T>G	ENSP00000406266.2:p.Ile2564Met
ENST00000513819.1:c.263+1685T>G	ENSP00000421504.1:n.263+1685T>G
ENST00000514335.1:n.1574T>G
ENST00000621733.1:c.1-3728T>G	ENSP00000480694.1:n.1-3728T>G
NM_015384.4:c.7692T>G	NP_056199.2:p.Ile2564Met
NM_133433.3:c.7692T>G	NP_597677.2:p.Ile2564Met
XM_005248280.2:c.7692T>G	XP_005248337.1:p.Ile2564Met
XM_005248282.3:c.6948T>G	XP_005248339.2:p.Ile2316Met
XM_006714467.2:c.7545T>G	XP_006714530.1:p.Ile2515Met
XM_006714468.1:c.7494T>G	XP_006714531.1:p.Ile2498Met
XM_011514014.1:c.7311T>G	XP_011512316.1:p.Ile2437Met
XM_011514015.1:c.*4T>G	XP_011512317.1:n.*4T>G
XM_005248280.3:c.7692T>G	XP_005248337.1:p.Ile2564Met
XM_005248282.5:c.7032T>G	XP_005248339.3:p.Ile2344Met
XM_006714468.2:c.7494T>G	XP_006714531.1:p.Ile2498Met
XM_017009329.1:c.7545T>G	XP_016864818.1:p.Ile2515Met
XM_017009330.2:c.6075T>G	XP_016864819.1:p.Ile2025Met
XM_017009331.1:c.6066T>G	XP_016864820.1:p.Ile2022Met
NM_133433.4:c.7692T>G MANE Select	NP_597677.2:p.Ile2564Met
NM_015384.5:c.7692T>G	NP_056199.2:p.Ile2564Met