Canonical Allele Identifier: CA2762882603

Gene: NFKB1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.102598574_102598575dup , CM000666.2:g.102598574_102598575dup	GRCh38
NC_000004.11:g.103519731_103519732dup , CM000666.1:g.103519731_103519732dup	GRCh37
NC_000004.10:g.103738769_103738770dup	NCBI36
NG_050628.1:g.102246_102247dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507079.6:c.1661+913_1661+914dup	ENSP00000426147.2:n.1661+913_1661+914dup
ENST00000509165.2:c.1637+913_1637+914dup	ENSP00000423877.2:n.1637+913_1637+914dup
ENST00000697794.1:c.*1278+913_*1278+914dup	ENSP00000513443.1:n.*1278+913_*1278+914dup
ENST00000697799.1:n.1134+913_1134+914dup
ENST00000698233.1:n.1366+913_1366+914dup
ENST00000226574.9:c.1637+913_1637+914dup MANE Select	ENSP00000226574.4:n.1637+913_1637+914dup
ENST00000652569.1:c.1613+913_1613+914dup
ENST00000652619.1:c.*164+913_*164+914dup	ENSP00000499031.1:n.*164+913_*164+914dup
ENST00000226574.8:c.1637+913_1637+914dup	ENSP00000226574.4:n.1637+913_1637+914dup
ENST00000394820.8:c.1634+913_1634+914dup	ENSP00000378297.4:n.1634+913_1634+914dup
ENST00000505458.5:c.1634+913_1634+914dup	ENSP00000424790.1:n.1634+913_1634+914dup
ENST00000600343.5:c.1094+913_1094+914dup	ENSP00000469340.1:n.1094+913_1094+914dup
NM_001165412.1:c.1634+913_1634+914dup	NP_001158884.1:n.1634+913_1634+914dup
NM_003998.3:c.1637+913_1637+914dup	NP_003989.2:n.1637+913_1637+914dup
XM_011532006.1:c.1658+913_1658+914dup	XP_011530308.1:n.1658+913_1658+914dup
XM_011532007.1:c.1634+913_1634+914dup	XP_011530309.1:n.1634+913_1634+914dup
XM_011532008.1:c.1478+913_1478+914dup	XP_011530310.1:n.1478+913_1478+914dup
XM_011532009.1:c.1241+913_1241+914dup	XP_011530311.1:n.1241+913_1241+914dup
XR_939027.1:n.3752_3753dup
NM_001319226.1:c.1634+913_1634+914dup	NP_001306155.1:n.1634+913_1634+914dup
XM_011532006.2:c.1658+913_1658+914dup	XP_011530308.1:n.1658+913_1658+914dup
XM_024454067.1:c.1661+913_1661+914dup	XP_024309835.1:n.1661+913_1661+914dup
XM_024454068.1:c.1637+913_1637+914dup	XP_024309836.1:n.1637+913_1637+914dup
XM_024454069.1:c.1502+913_1502+914dup	XP_024309837.1:n.1502+913_1502+914dup
NM_003998.4:c.1637+913_1637+914dup MANE Select	NP_003989.2:n.1637+913_1637+914dup
NM_001165412.2:c.1634+913_1634+914dup	NP_001158884.1:n.1634+913_1634+914dup
NM_001319226.2:c.1634+913_1634+914dup	NP_001306155.1:n.1634+913_1634+914dup
NM_001382625.1:c.1637+913_1637+914dup	NP_001369554.1:n.1637+913_1637+914dup
NM_001382626.1:c.1637+913_1637+914dup	NP_001369555.1:n.1637+913_1637+914dup
NM_001382627.1:c.1634+913_1634+914dup	NP_001369556.1:n.1634+913_1634+914dup
NM_001382628.1:c.1595+913_1595+914dup	NP_001369557.1:n.1595+913_1595+914dup