Canonical Allele Identifier: CA9073126
Gene: TLE6 HGNC NCBI

Linked Data

dbSNP Id: rs767222404
gnomAD v2: 19-2993572-C-G
gnomAD v4: 19-2993574-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.2993574C>G , CM000681.2:g.2993574C>G GRCh38
NC_000019.9:g.2993572C>G , CM000681.1:g.2993572C>G GRCh37
NC_000019.8:g.2944572C>G NCBI36
NG_051563.1:g.21160C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000246112.9:c.1529C>G MANE Select ENSP00000246112.3:p.Ser510Cys
ENST00000246112.8:c.1529C>G ENSP00000246112.3:p.Ser510Cys
ENST00000452088.5:c.1160C>G ENSP00000406893.1:p.Ser387Cys
ENST00000497878.5:n.1222C>G
ENST00000617937.4:c.1158C>G ENSP00000483606.2:p.Leu386=
NM_001143986.1:c.1529C>G NP_001137458.1:p.Ser510Cys
NM_024760.2:c.1160C>G NP_079036.1:p.Ser387Cys
XM_005259645.2:c.1529C>G XP_005259702.1:p.Ser510Cys
XM_011528300.1:c.1529C>G XP_011526602.1:p.Ser510Cys
XM_011528301.1:c.1160C>G XP_011526603.1:p.Ser387Cys
XM_011528302.1:c.1160C>G XP_011526604.1:p.Ser387Cys
XM_011528303.1:c.1160C>G XP_011526605.1:p.Ser387Cys
XM_011528304.1:c.1160C>G XP_011526606.1:p.Ser387Cys
XM_011528305.1:c.1010C>G XP_011526607.1:p.Ser337Cys
XM_011528306.1:c.1010C>G XP_011526608.1:p.Ser337Cys
XM_011528307.1:c.1010C>G XP_011526609.1:p.Ser337Cys
XM_011528300.2:c.1529C>G XP_011526602.1:p.Ser510Cys
XM_011528301.2:c.1160C>G XP_011526603.1:p.Ser387Cys
XM_024451722.1:c.1160C>G XP_024307490.1:p.Ser387Cys
XM_024451723.1:c.1160C>G XP_024307491.1:p.Ser387Cys
XM_024451724.1:c.1010C>G XP_024307492.1:p.Ser337Cys
NM_001143986.2:c.1529C>G MANE Select NP_001137458.1:p.Ser510Cys
NM_024760.3:c.1160C>G NP_079036.1:p.Ser387Cys