Canonical Allele Identifier: CA241174729

Gene: TMTC3

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.88148143C>T , CM000674.2:g.88148143C>T	GRCh38
NC_000012.11:g.88541920C>T , CM000674.1:g.88541920C>T	GRCh37
NC_000012.10:g.87066051C>T	NCBI36
NG_021187.1:g.10848C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266712.11:c.-28-145C>T MANE Select	ENSP00000266712.6:n.-28-145C>T
ENST00000266712.10:c.-28-145C>T	ENSP00000266712.6:n.-28-145C>T
ENST00000547034.5:c.-28-145C>T	ENSP00000448733.1:n.-28-145C>T
ENST00000549011.5:c.-28-145C>T	ENSP00000447640.1:n.-28-145C>T
ENST00000551088.1:c.-28-145C>T	ENSP00000448566.1:n.-28-145C>T
NM_181783.3:c.-28-145C>T	NP_861448.2:n.-28-145C>T
XM_011537980.1:c.-28-145C>T	XP_011536282.1:n.-28-145C>T
NM_001366574.1:c.-77-276C>T	NP_001353503.1:n.-77-276C>T
NM_001366579.1:c.-28-145C>T	NP_001353508.1:n.-28-145C>T
NM_001366580.1:c.-78-5148C>T	NP_001353509.1:n.-78-5148C>T
NM_001366583.1:c.-286+5656C>T	NP_001353512.1:n.-286+5656C>T
NR_159381.1:n.182-145C>T
NM_181783.4:c.-28-145C>T MANE Select	NP_861448.2:n.-28-145C>T