Canonical Allele Identifier: CA804710755

Gene: CD14 TMCO6

Linked Data

• dbSNP Id: rs1204060722
• gnomAD v4: 5-140633210-CCTGGGATGTCATTCAGTTCCCTCCT-C
• MyVariant Identifiers: chr5:g.140012796_140012820del (hg19) ; chr5:g.140633211_140633235del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140633214_140633238del , CM000667.2:g.140633214_140633238del	GRCh38
NC_000005.9:g.140012799_140012823del , CM000667.1:g.140012799_140012823del	GRCh37
NC_000005.8:g.139992983_139993007del	NCBI36
NG_023178.1:g.5467_5491del

Transcript Alleles

HGVS	Amino-acid change
ENST00000498971.7:c.-121-43_-121-19del (CD14)	ENSP00000426543.2:n.-121-43_-121-19del
ENST00000512545.2:c.-164_-140del (CD14)	ENSP00000425447.2:n.-164_-140del
ENST00000519715.2:c.-121-43_-121-19del (CD14)	ENSP00000430884.2:n.-121-43_-121-19del
ENST00000302014.10:c.-164_-140del (CD14)	ENSP00000304236.6:n.-164_-140del
ENST00000401743.6:c.-164_-140del (CD14)	ENSP00000385519.2:n.-164_-140del
ENST00000498971.6:c.-121-43_-121-19del (CD14)	ENSP00000426543.1:n.-121-43_-121-19del
ENST00000512545.1:c.-164_-140del (CD14)	ENSP00000425447.1:n.-164_-140del
ENST00000519715.1:c.-121-43_-121-19del (CD14)	ENSP00000430884.1:n.-121-43_-121-19del
NM_000591.3:c.-164_-140del (CD14)	NP_000582.1:n.-164_-140del
NM_001040021.2:c.-121-43_-121-19del (CD14)	NP_001035110.1:n.-121-43_-121-19del
NM_001174104.1:c.-164_-140del (CD14)	NP_001167575.1:n.-164_-140del
NM_001174105.1:c.-121-43_-121-19del (CD14)	NP_001167576.1:n.-121-43_-121-19del
XM_011537665.1:c.-129-8451_-129-8427del (TMCO6)	XP_011535967.1:n.-129-8451_-129-8427del
XM_011537665.2:c.-129-8451_-129-8427del (TMCO6)	XP_011535967.1:n.-129-8451_-129-8427del
NM_001040021.3:c.-121-43_-121-19del (CD14)	NP_001035110.1:n.-121-43_-121-19del
NM_001174105.2:c.-121-43_-121-19del (CD14)	NP_001167576.1:n.-121-43_-121-19del
NM_001174104.2:c.-164_-140del (CD14)	NP_001167575.1:n.-164_-140del