Canonical Allele Identifier: CA1539601805

Gene: NIPBL

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.37001225_37001228delinsTTTC , CM000667.2:g.37001225_37001228delinsTTTC	GRCh38
NC_000005.9:g.37001327_37001330delinsTTTC , CM000667.1:g.37001327_37001330delinsTTTC	GRCh37
NC_000005.8:g.37037084_37037087delinsTTTC	NCBI36
NG_006987.1:g.129343_129346delinsTTTC
NG_006987.2:g.129343_129346delinsTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000282516.13:c.3664+147_3664+150delinsTTTC MANE Select	ENSP00000282516.8:n.3664+147_3664+150delinsTTTC
ENST00000652901.1:c.3664+147_3664+150delinsTTTC	ENSP00000499536.1:n.3664+147_3664+150delinsTTTC
ENST00000282516.12:c.3664+147_3664+150delinsTTTC	ENSP00000282516.8:n.3664+147_3664+150delinsTTTC
ENST00000448238.2:c.3664+147_3664+150delinsTTTC	ENSP00000406266.2:n.3664+147_3664+150delinsTTTC
ENST00000621733.1:c.1-63353_1-63350delinsTTTC	ENSP00000480694.1:n.1-63353_1-63350delinsTTTC
NM_015384.4:c.3664+147_3664+150delinsTTTC	NP_056199.2:n.3664+147_3664+150delinsTTTC
NM_133433.3:c.3664+147_3664+150delinsTTTC	NP_597677.2:n.3664+147_3664+150delinsTTTC
XM_005248280.2:c.3664+147_3664+150delinsTTTC	XP_005248337.1:n.3664+147_3664+150delinsTTTC
XM_005248282.3:c.2920+147_2920+150delinsTTTC	XP_005248339.2:n.2920+147_2920+150delinsTTTC
XM_006714467.2:c.3664+147_3664+150delinsTTTC	XP_006714530.1:n.3664+147_3664+150delinsTTTC
XM_006714468.1:c.3466+147_3466+150delinsTTTC	XP_006714531.1:n.3466+147_3466+150delinsTTTC
XM_011514014.1:c.3283+147_3283+150delinsTTTC	XP_011512316.1:n.3283+147_3283+150delinsTTTC
XM_011514015.1:c.3664+147_3664+150delinsTTTC	XP_011512317.1:n.3664+147_3664+150delinsTTTC
XM_005248280.3:c.3664+147_3664+150delinsTTTC	XP_005248337.1:n.3664+147_3664+150delinsTTTC
XM_005248282.5:c.3004+147_3004+150delinsTTTC	XP_005248339.3:n.3004+147_3004+150delinsTTTC
XM_006714468.2:c.3466+147_3466+150delinsTTTC	XP_006714531.1:n.3466+147_3466+150delinsTTTC
XM_017009329.1:c.3664+147_3664+150delinsTTTC	XP_016864818.1:n.3664+147_3664+150delinsTTTC
XM_017009330.2:c.2047+147_2047+150delinsTTTC	XP_016864819.1:n.2047+147_2047+150delinsTTTC
XM_017009331.1:c.2038+147_2038+150delinsTTTC	XP_016864820.1:n.2038+147_2038+150delinsTTTC
NM_133433.4:c.3664+147_3664+150delinsTTTC MANE Select	NP_597677.2:n.3664+147_3664+150delinsTTTC
NM_015384.5:c.3664+147_3664+150delinsTTTC	NP_056199.2:n.3664+147_3664+150delinsTTTC