Canonical Allele Identifier: CA2575244168

Gene: TMTC3

Linked Data

• gnomAD v4: 12-88188801-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88188801C>A , CM000674.2:g.88188801C>A	GRCh38
NC_000012.11:g.88582578C>A , CM000674.1:g.88582578C>A	GRCh37
NC_000012.10:g.87106709C>A	NCBI36
NG_021187.1:g.51506C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000266712.11:c.1433-42C>A MANE Select	ENSP00000266712.6:n.1433-42C>A
ENST00000266712.10:c.1433-42C>A	ENSP00000266712.6:n.1433-42C>A
ENST00000547034.5:c.*336-42C>A	ENSP00000448733.1:n.*336-42C>A
NM_181783.3:c.1433-42C>A	NP_861448.2:n.1433-42C>A
XM_005268683.3:c.287-42C>A	XP_005268740.1:n.287-42C>A
XM_011537980.1:c.1214-42C>A	XP_011536282.1:n.1214-42C>A
XM_011537981.1:c.200-42C>A	XP_011536283.1:n.200-42C>A
NM_001366574.1:c.1253-42C>A	NP_001353503.1:n.1253-42C>A
NM_001366579.1:c.1214-42C>A	NP_001353508.1:n.1214-42C>A
NM_001366580.1:c.1166-42C>A	NP_001353509.1:n.1166-42C>A
NM_001366583.1:c.740-42C>A	NP_001353512.1:n.740-42C>A
NR_159381.1:n.1766-42C>A
NM_181783.4:c.1433-42C>A MANE Select	NP_861448.2:n.1433-42C>A