Canonical Allele Identifier: CA2675601477

Gene: CD14 TMCO6

Linked Data

• gnomAD v4: 5-140633334-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140633334G>C , CM000667.2:g.140633334G>C	GRCh38
NC_000005.9:g.140012919G>C , CM000667.1:g.140012919G>C	GRCh37
NC_000005.8:g.139993103G>C	NCBI36
NG_023178.1:g.5368C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498971.7:c.-121-142C>G (CD14)	ENSP00000426543.2:n.-121-142C>G
ENST00000512545.2:c.-221-42C>G (CD14)	ENSP00000425447.2:n.-221-42C>G
ENST00000519715.2:c.-121-142C>G (CD14)	ENSP00000430884.2:n.-121-142C>G
ENST00000302014.10:c.-263C>G (CD14)	ENSP00000304236.6:n.-263C>G
ENST00000401743.6:c.-221-42C>G (CD14)	ENSP00000385519.2:n.-221-42C>G
ENST00000498971.6:c.-121-142C>G (CD14)	ENSP00000426543.1:n.-121-142C>G
ENST00000512545.1:c.-221-42C>G (CD14)	ENSP00000425447.1:n.-221-42C>G
ENST00000519715.1:c.-121-142C>G (CD14)	ENSP00000430884.1:n.-121-142C>G
NM_000591.3:c.-263C>G (CD14)	NP_000582.1:n.-263C>G
NM_001040021.2:c.-121-142C>G (CD14)	NP_001035110.1:n.-121-142C>G
NM_001174104.1:c.-221-42C>G (CD14)	NP_001167575.1:n.-221-42C>G
NM_001174105.1:c.-121-142C>G (CD14)	NP_001167576.1:n.-121-142C>G
XM_011537665.1:c.-129-8331G>C (TMCO6)	XP_011535967.1:n.-129-8331G>C
XM_011537665.2:c.-129-8331G>C (TMCO6)	XP_011535967.1:n.-129-8331G>C
NM_001040021.3:c.-121-142C>G (CD14)	NP_001035110.1:n.-121-142C>G
NM_001174105.2:c.-121-142C>G (CD14)	NP_001167576.1:n.-121-142C>G
NM_001174104.2:c.-221-42C>G (CD14)	NP_001167575.1:n.-221-42C>G