Canonical Allele Identifier: CA2052966159
Gene: TMTC3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88188783T= , CM000674.2:g.88188783T= GRCh38
NC_000012.11:g.88582560T= , CM000674.1:g.88582560T= GRCh37
NC_000012.10:g.87106691T= NCBI36
NG_021187.1:g.51488T=

Transcript Alleles

HGVS Amino-acid change
ENST00000266712.11:c.1433-60T= MANE Select ENSP00000266712.6:n.1433-60T=
ENST00000266712.10:c.1433-60T= ENSP00000266712.6:n.1433-60T=
ENST00000547034.5:c.*336-60T= ENSP00000448733.1:n.*336-60T=
NM_181783.3:c.1433-60T= NP_861448.2:n.1433-60T=
XM_005268683.3:c.287-60T= XP_005268740.1:n.287-60T=
XM_011537980.1:c.1214-60T= XP_011536282.1:n.1214-60T=
XM_011537981.1:c.200-60T= XP_011536283.1:n.200-60T=
NM_001366574.1:c.1253-60T= NP_001353503.1:n.1253-60T=
NM_001366579.1:c.1214-60T= NP_001353508.1:n.1214-60T=
NM_001366580.1:c.1166-60T= NP_001353509.1:n.1166-60T=
NM_001366583.1:c.740-60T= NP_001353512.1:n.740-60T=
NR_159381.1:n.1766-60T=
NM_181783.4:c.1433-60T= MANE Select NP_861448.2:n.1433-60T=