Canonical Allele Identifier: CA2404069446

Gene: NCF4 NCF4-AS1

Linked Data

• dbSNP Id: rs1939794084

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.36862347_36862358del , CM000684.2:g.36862347_36862358del	GRCh38
NC_000022.10:g.37258389_37258400del , CM000684.1:g.37258389_37258400del	GRCh37
NC_000022.9:g.35588335_35588346del	NCBI36
NG_023400.1:g.6360_6371del , LRG_159:g.6360_6371del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248899.11:c.32+1144_32+1155del (NCF4) MANE Select	ENSP00000248899.6:n.32+1144_32+1155del
ENST00000397147.7:c.32+1144_32+1155del (NCF4)	ENSP00000380334.4:n.32+1144_32+1155del
ENST00000650827.1:c.-318_-307del (NCF4)	ENSP00000498212.1:n.-318_-307del
ENST00000248899.10:c.32+1144_32+1155del (NCF4)	ENSP00000248899.6:n.32+1144_32+1155del
ENST00000397147.6:c.32+1144_32+1155del (NCF4)	ENSP00000380334.4:n.32+1144_32+1155del
ENST00000447071.5:c.-193+1144_-193+1155del (NCF4)	ENSP00000414958.1:n.-193+1144_-193+1155del
NM_000631.4:c.32+1144_32+1155del (NCF4)	NP_000622.2:n.32+1144_32+1155del
NM_013416.3:c.32+1144_32+1155del , LRG_159t1:c.32+1144_32+1155del (NCF4)	NP_038202.2:n.32+1144_32+1155del
XM_011530198.1:c.-308_-297del (NCF4)	XP_011528500.1:n.-308_-297del
XM_011530199.1:c.97+532_97+543del (NCF4)	XP_011528501.1:n.97+532_97+543del
NR_147197.1:n.351+7738_351+7749del (NCF4-AS1)
XM_017028808.1:c.-278+532_-278+543del (NCF4)	XP_016884297.1:n.-278+532_-278+543del
NM_000631.5:c.32+1144_32+1155del (NCF4) MANE Select	NP_000622.2:n.32+1144_32+1155del
NM_013416.4:c.32+1144_32+1155del (NCF4)	NP_038202.2:n.32+1144_32+1155del