Canonical Allele Identifier: CA804710765

Gene: CD14 TMCO6

Linked Data

• dbSNP Id: rs1469664795
• gnomAD v3: 5-140633250-C-T
• gnomAD v4: 5-140633250-C-T
• MyVariant Identifiers: chr5:g.140012835C>T (hg19) ; chr5:g.140633250C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.140633250C>T , CM000667.2:g.140633250C>T	GRCh38
NC_000005.9:g.140012835C>T , CM000667.1:g.140012835C>T	GRCh37
NC_000005.8:g.139993019C>T	NCBI36
NG_023178.1:g.5452G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000498971.7:c.-121-58G>A (CD14)	ENSP00000426543.2:n.-121-58G>A
ENST00000512545.2:c.-179G>A (CD14)	ENSP00000425447.2:n.-179G>A
ENST00000519715.2:c.-121-58G>A (CD14)	ENSP00000430884.2:n.-121-58G>A
ENST00000302014.10:c.-179G>A (CD14)	ENSP00000304236.6:n.-179G>A
ENST00000401743.6:c.-179G>A (CD14)	ENSP00000385519.2:n.-179G>A
ENST00000498971.6:c.-121-58G>A (CD14)	ENSP00000426543.1:n.-121-58G>A
ENST00000512545.1:c.-179G>A (CD14)	ENSP00000425447.1:n.-179G>A
ENST00000519715.1:c.-121-58G>A (CD14)	ENSP00000430884.1:n.-121-58G>A
NM_000591.3:c.-179G>A (CD14)	NP_000582.1:n.-179G>A
NM_001040021.2:c.-121-58G>A (CD14)	NP_001035110.1:n.-121-58G>A
NM_001174104.1:c.-179G>A (CD14)	NP_001167575.1:n.-179G>A
NM_001174105.1:c.-121-58G>A (CD14)	NP_001167576.1:n.-121-58G>A
XM_011537665.1:c.-129-8415C>T (TMCO6)	XP_011535967.1:n.-129-8415C>T
XM_011537665.2:c.-129-8415C>T (TMCO6)	XP_011535967.1:n.-129-8415C>T
NM_001040021.3:c.-121-58G>A (CD14)	NP_001035110.1:n.-121-58G>A
NM_001174105.2:c.-121-58G>A (CD14)	NP_001167576.1:n.-121-58G>A
NM_001174104.2:c.-179G>A (CD14)	NP_001167575.1:n.-179G>A