Canonical Allele Identifier: CA433458592

Gene: TMIE

Linked Data

• MyVariant Identifiers: chr3:g.46747282C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46705792C>G , CM000665.2:g.46705792C>G	GRCh38
NC_000003.11:g.46747282C>G , CM000665.1:g.46747282C>G	GRCh37
NC_000003.10:g.46722286C>G	NCBI36
NG_011628.1:g.9460C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.96C>G MANE Select	ENSP00000494576.2:p.Pro32=
ENST00000644830.1:c.-64C>G	ENSP00000495111.1:n.-64C>G
ENST00000326431.3:c.96C>G	ENSP00000324775.3:p.Pro32=
NM_147196.2:c.96C>G	NP_671729.2:p.Pro32=
XM_006713097.2:c.-64C>G	XP_006713160.1:n.-64C>G
XM_011533574.1:c.-64C>G	XP_011531876.1:n.-64C>G
XM_006713097.4:c.-64C>G	XP_006713160.1:n.-64C>G
XM_024453446.1:c.-64C>G	XP_024309214.1:n.-64C>G
NM_001370524.1:c.-64C>G	NP_001357453.1:n.-64C>G
NM_001370525.1:c.-64C>G	NP_001357454.1:n.-64C>G
NM_147196.3:c.96C>G MANE Select	NP_671729.2:p.Pro32=