Canonical Allele Identifier: CA2052966167
Gene: TMTC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88188797A= , CM000674.2:g.88188797A= GRCh38
NC_000012.11:g.88582574A= , CM000674.1:g.88582574A= GRCh37
NC_000012.10:g.87106705A= NCBI36
NG_021187.1:g.51502A=

Transcript Alleles

HGVS Amino-acid change
ENST00000266712.11:c.1433-46A= MANE Select ENSP00000266712.6:n.1433-46A=
ENST00000266712.10:c.1433-46A= ENSP00000266712.6:n.1433-46A=
ENST00000547034.5:c.*336-46A= ENSP00000448733.1:n.*336-46A=
NM_181783.3:c.1433-46A= NP_861448.2:n.1433-46A=
XM_005268683.3:c.287-46A= XP_005268740.1:n.287-46A=
XM_011537980.1:c.1214-46A= XP_011536282.1:n.1214-46A=
XM_011537981.1:c.200-46A= XP_011536283.1:n.200-46A=
NM_001366574.1:c.1253-46A= NP_001353503.1:n.1253-46A=
NM_001366579.1:c.1214-46A= NP_001353508.1:n.1214-46A=
NM_001366580.1:c.1166-46A= NP_001353509.1:n.1166-46A=
NM_001366583.1:c.740-46A= NP_001353512.1:n.740-46A=
NR_159381.1:n.1766-46A=
NM_181783.4:c.1433-46A= MANE Select NP_861448.2:n.1433-46A=