Canonical Allele Identifier: CA1451832675

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.38830014T= , CM000666.2:g.38830014T= GRCh38
NC_000004.11:g.38831635T= , CM000666.1:g.38831635T= GRCh37
NC_000004.10:g.38508030T= NCBI36
NG_028087.1:g.31804A=

Transcript Alleles

HGVS Amino-acid change
ENST00000381950.2:c.-64-477A= (TLR6) ENSP00000371376.1:n.-64-477A=
ENST00000508254.6:c.-64-477A= (TLR6) MANE Select ENSP00000424718.2:n.-64-477A=
ENST00000436693.6:c.-64-477A= (TLR6) ENSP00000389600.2:n.-64-477A=
ENST00000506146.5:c.-352-24821A= (TLR1) ENSP00000423725.1:n.-352-24821A=
ENST00000508254.5:c.-64-477A= (TLR6) ENSP00000424718.1:n.-64-477A=
ENST00000514655.1:c.-64-477A= (TLR6) ENSP00000423326.1:n.-64-477A=
NM_006068.4:c.-64-477A= (TLR6) NP_006059.2:n.-64-477A=
XM_005262637.3:c.-64-477A= (TLR6) XP_005262694.1:n.-64-477A=
XM_011513612.1:c.-64-477A= (TLR6) XP_011511914.1:n.-64-477A=
XM_011513613.1:c.-64-477A= (TLR6) XP_011511915.1:n.-64-477A=
XM_011513614.1:c.-64-477A= (TLR6) XP_011511916.1:n.-64-477A=
XM_005262637.5:c.-64-477A= (TLR6) XP_005262694.1:n.-64-477A=
XM_011513613.3:c.-64-477A= (TLR6) XP_011511915.1:n.-64-477A=
XM_011513614.3:c.-64-477A= (TLR6) XP_011511916.1:n.-64-477A=
XM_024453873.1:c.-64-477A= (TLR6) XP_024309641.1:n.-64-477A=
NM_006068.5:c.-64-477A= (TLR6) MANE Select NP_006059.2:n.-64-477A=
NM_001394553.1:c.-64-477A= (TLR6) NP_001381482.1:n.-64-477A=