Canonical Allele Identifier: CA2620113608

Gene: TMTC3

Linked Data

• gnomAD v4: 12-88188799-ATCAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88188801_88188804del , CM000674.2:g.88188801_88188804del	GRCh38
NC_000012.11:g.88582578_88582581del , CM000674.1:g.88582578_88582581del	GRCh37
NC_000012.10:g.87106709_87106712del	NCBI36
NG_021187.1:g.51506_51509del

Transcript Alleles

HGVS	Amino-acid change
ENST00000266712.11:c.1433-42_1433-39del MANE Select	ENSP00000266712.6:n.1433-42_1433-39del
ENST00000266712.10:c.1433-42_1433-39del	ENSP00000266712.6:n.1433-42_1433-39del
ENST00000547034.5:c.*336-42_*336-39del	ENSP00000448733.1:n.*336-42_*336-39del
NM_181783.3:c.1433-42_1433-39del	NP_861448.2:n.1433-42_1433-39del
XM_005268683.3:c.287-42_287-39del	XP_005268740.1:n.287-42_287-39del
XM_011537980.1:c.1214-42_1214-39del	XP_011536282.1:n.1214-42_1214-39del
XM_011537981.1:c.200-42_200-39del	XP_011536283.1:n.200-42_200-39del
NM_001366574.1:c.1253-42_1253-39del	NP_001353503.1:n.1253-42_1253-39del
NM_001366579.1:c.1214-42_1214-39del	NP_001353508.1:n.1214-42_1214-39del
NM_001366580.1:c.1166-42_1166-39del	NP_001353509.1:n.1166-42_1166-39del
NM_001366583.1:c.740-42_740-39del	NP_001353512.1:n.740-42_740-39del
NR_159381.1:n.1766-42_1766-39del
NM_181783.4:c.1433-42_1433-39del MANE Select	NP_861448.2:n.1433-42_1433-39del