Canonical Allele Identifier: CA2620113558

Gene: TMTC3

Linked Data

• gnomAD v4: 12-88188777-TTTCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88188780_88188783del , CM000674.2:g.88188780_88188783del	GRCh38
NC_000012.11:g.88582557_88582560del , CM000674.1:g.88582557_88582560del	GRCh37
NC_000012.10:g.87106688_87106691del	NCBI36
NG_021187.1:g.51485_51488del

Transcript Alleles

HGVS	Amino-acid change
ENST00000266712.11:c.1433-63_1433-60del MANE Select	ENSP00000266712.6:n.1433-63_1433-60del
ENST00000266712.10:c.1433-63_1433-60del	ENSP00000266712.6:n.1433-63_1433-60del
ENST00000547034.5:c.*336-63_*336-60del	ENSP00000448733.1:n.*336-63_*336-60del
NM_181783.3:c.1433-63_1433-60del	NP_861448.2:n.1433-63_1433-60del
XM_005268683.3:c.287-63_287-60del	XP_005268740.1:n.287-63_287-60del
XM_011537980.1:c.1214-63_1214-60del	XP_011536282.1:n.1214-63_1214-60del
XM_011537981.1:c.200-63_200-60del	XP_011536283.1:n.200-63_200-60del
NM_001366574.1:c.1253-63_1253-60del	NP_001353503.1:n.1253-63_1253-60del
NM_001366579.1:c.1214-63_1214-60del	NP_001353508.1:n.1214-63_1214-60del
NM_001366580.1:c.1166-63_1166-60del	NP_001353509.1:n.1166-63_1166-60del
NM_001366583.1:c.740-63_740-60del	NP_001353512.1:n.740-63_740-60del
NR_159381.1:n.1766-63_1766-60del
NM_181783.4:c.1433-63_1433-60del MANE Select	NP_861448.2:n.1433-63_1433-60del