Canonical Allele Identifier: CA563329121

Gene: CD14 TMCO6

Linked Data

• dbSNP Id: rs1231853804
• gnomAD v2: 5-140012824-T-C
• gnomAD v4: 5-140633239-T-C
• MyVariant Identifiers: chr5:g.140012824T>C (hg19) ; chr5:g.140633239T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140633239T>C , CM000667.2:g.140633239T>C	GRCh38
NC_000005.9:g.140012824T>C , CM000667.1:g.140012824T>C	GRCh37
NC_000005.8:g.139993008T>C	NCBI36
NG_023178.1:g.5463A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498971.7:c.-121-47A>G (CD14)	ENSP00000426543.2:n.-121-47A>G
ENST00000512545.2:c.-168A>G (CD14)	ENSP00000425447.2:n.-168A>G
ENST00000519715.2:c.-121-47A>G (CD14)	ENSP00000430884.2:n.-121-47A>G
ENST00000302014.10:c.-168A>G (CD14)	ENSP00000304236.6:n.-168A>G
ENST00000401743.6:c.-168A>G (CD14)	ENSP00000385519.2:n.-168A>G
ENST00000498971.6:c.-121-47A>G (CD14)	ENSP00000426543.1:n.-121-47A>G
ENST00000512545.1:c.-168A>G (CD14)	ENSP00000425447.1:n.-168A>G
ENST00000519715.1:c.-121-47A>G (CD14)	ENSP00000430884.1:n.-121-47A>G
NM_000591.3:c.-168A>G (CD14)	NP_000582.1:n.-168A>G
NM_001040021.2:c.-121-47A>G (CD14)	NP_001035110.1:n.-121-47A>G
NM_001174104.1:c.-168A>G (CD14)	NP_001167575.1:n.-168A>G
NM_001174105.1:c.-121-47A>G (CD14)	NP_001167576.1:n.-121-47A>G
XM_011537665.1:c.-129-8426T>C (TMCO6)	XP_011535967.1:n.-129-8426T>C
XM_011537665.2:c.-129-8426T>C (TMCO6)	XP_011535967.1:n.-129-8426T>C
NM_001040021.3:c.-121-47A>G (CD14)	NP_001035110.1:n.-121-47A>G
NM_001174105.2:c.-121-47A>G (CD14)	NP_001167576.1:n.-121-47A>G
NM_001174104.2:c.-168A>G (CD14)	NP_001167575.1:n.-168A>G