Canonical Allele Identifier: CA1451828400

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38828729A= , CM000666.2:g.38828729A= GRCh38
NC_000004.11:g.38830350A= , CM000666.1:g.38830350A= GRCh37
NC_000004.10:g.38506745A= NCBI36
NG_028087.1:g.33089T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000381950.2:c.745T= (TLR6) ENSP00000371376.1:p.Ser249=
ENST00000508254.6:c.745T= (TLR6) MANE Select ENSP00000424718.2:p.Ser249=
ENST00000381950.1:c.745T= (TLR6) ENSP00000371376.1:p.Ser249=
ENST00000436693.6:c.745T= (TLR6) ENSP00000389600.2:p.Ser249=
ENST00000506146.5:c.-352-23536T= (TLR1) ENSP00000423725.1:n.-352-23536T=
ENST00000610323.2:c.745T= (TLR6) ENSP00000480266.1:p.Ser249=
NM_006068.4:c.745T= (TLR6) NP_006059.2:p.Ser249=
XM_005262637.3:c.745T= (TLR6) XP_005262694.1:p.Ser249=
XM_011513612.1:c.745T= (TLR6) XP_011511914.1:p.Ser249=
XM_011513613.1:c.745T= (TLR6) XP_011511915.1:p.Ser249=
XM_011513614.1:c.745T= (TLR6) XP_011511916.1:p.Ser249=
XM_005262637.5:c.745T= (TLR6) XP_005262694.1:p.Ser249=
XM_011513613.3:c.745T= (TLR6) XP_011511915.1:p.Ser249=
XM_011513614.3:c.745T= (TLR6) XP_011511916.1:p.Ser249=
XM_024453873.1:c.745T= (TLR6) XP_024309641.1:p.Ser249=
NM_006068.5:c.745T= (TLR6) MANE Select NP_006059.2:p.Ser249=
NM_001394553.1:c.745T= (TLR6) NP_001381482.1:p.Ser249=