Canonical Allele Identifier: CA352480636

Gene: TMIE

Linked Data

• MyVariant Identifiers: chr3:g.46750663A>C (hg19) ; chr3:g.46709173A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46709173A>C , CM000665.2:g.46709173A>C	GRCh38
NC_000003.11:g.46750663A>C , CM000665.1:g.46750663A>C	GRCh37
NC_000003.10:g.46725667A>C	NCBI36
NG_011628.1:g.12841A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.259A>C MANE Select	ENSP00000494576.2:p.Lys87Gln
ENST00000644830.1:c.100A>C	ENSP00000495111.1:p.Lys34Gln
ENST00000651652.1:c.157A>C	ENSP00000498953.1:p.Lys53Gln
ENST00000326431.3:c.259A>C	ENSP00000324775.3:p.Lys87Gln
NM_147196.2:c.259A>C	NP_671729.2:p.Lys87Gln
XM_006713097.2:c.100A>C	XP_006713160.1:p.Lys34Gln
XM_011533574.1:c.100A>C	XP_011531876.1:p.Lys34Gln
XM_006713097.4:c.100A>C	XP_006713160.1:p.Lys34Gln
XM_024453446.1:c.100A>C	XP_024309214.1:p.Lys34Gln
NM_001370524.1:c.100A>C	NP_001357453.1:p.Lys34Gln
NM_001370525.1:c.100A>C	NP_001357454.1:p.Lys34Gln
NM_147196.3:c.259A>C MANE Select	NP_671729.2:p.Lys87Gln