Canonical Allele Identifier: CA2575244165
Gene: TMTC3 HGNC NCBI

Linked Data

gnomAD v4: 12-88188786-G-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.88188786G>A , CM000674.2:g.88188786G>A GRCh38
NC_000012.11:g.88582563G>A , CM000674.1:g.88582563G>A GRCh37
NC_000012.10:g.87106694G>A NCBI36
NG_021187.1:g.51491G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000266712.11:c.1433-57G>A MANE Select ENSP00000266712.6:n.1433-57G>A
ENST00000266712.10:c.1433-57G>A ENSP00000266712.6:n.1433-57G>A
ENST00000547034.5:c.*336-57G>A ENSP00000448733.1:n.*336-57G>A
NM_181783.3:c.1433-57G>A NP_861448.2:n.1433-57G>A
XM_005268683.3:c.287-57G>A XP_005268740.1:n.287-57G>A
XM_011537980.1:c.1214-57G>A XP_011536282.1:n.1214-57G>A
XM_011537981.1:c.200-57G>A XP_011536283.1:n.200-57G>A
NM_001366574.1:c.1253-57G>A NP_001353503.1:n.1253-57G>A
NM_001366579.1:c.1214-57G>A NP_001353508.1:n.1214-57G>A
NM_001366580.1:c.1166-57G>A NP_001353509.1:n.1166-57G>A
NM_001366583.1:c.740-57G>A NP_001353512.1:n.740-57G>A
NR_159381.1:n.1766-57G>A
NM_181783.4:c.1433-57G>A MANE Select NP_861448.2:n.1433-57G>A
Search 100 bp 5'
Search 100 bp 3'