Canonical Allele Identifier: CA2675601476

Gene: CD14 TMCO6

Linked Data

• gnomAD v4: 5-140633334-G-A

Genomic Alleles

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

Transcript Alleles

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