Canonical Allele Identifier: CA2052966177
Gene: TMTC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88188819C= , CM000674.2:g.88188819C= GRCh38
NC_000012.11:g.88582596C= , CM000674.1:g.88582596C= GRCh37
NC_000012.10:g.87106727C= NCBI36
NG_021187.1:g.51524C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000266712.11:c.1433-24C= MANE Select ENSP00000266712.6:n.1433-24C=
ENST00000266712.10:c.1433-24C= ENSP00000266712.6:n.1433-24C=
ENST00000547034.5:c.*336-24C= ENSP00000448733.1:n.*336-24C=
NM_181783.3:c.1433-24C= NP_861448.2:n.1433-24C=
XM_005268683.3:c.287-24C= XP_005268740.1:n.287-24C=
XM_011537980.1:c.1214-24C= XP_011536282.1:n.1214-24C=
XM_011537981.1:c.200-24C= XP_011536283.1:n.200-24C=
NM_001366574.1:c.1253-24C= NP_001353503.1:n.1253-24C=
NM_001366579.1:c.1214-24C= NP_001353508.1:n.1214-24C=
NM_001366580.1:c.1166-24C= NP_001353509.1:n.1166-24C=
NM_001366583.1:c.740-24C= NP_001353512.1:n.740-24C=
NR_159381.1:n.1766-24C=
NM_181783.4:c.1433-24C= MANE Select NP_861448.2:n.1433-24C=