Canonical Allele Identifier: CA433459101

Gene: TMIE

Linked Data

• MyVariant Identifiers: chr3:g.46750653A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46709163A>C , CM000665.2:g.46709163A>C	GRCh38
NC_000003.11:g.46750653A>C , CM000665.1:g.46750653A>C	GRCh37
NC_000003.10:g.46725657A>C	NCBI36
NG_011628.1:g.12831A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000643606.3:c.249A>C MANE Select	ENSP00000494576.2:p.Pro83=
ENST00000644830.1:c.90A>C	ENSP00000495111.1:p.Pro30=
ENST00000651652.1:c.147A>C	ENSP00000498953.1:p.Pro49=
ENST00000326431.3:c.249A>C	ENSP00000324775.3:p.Pro83=
NM_147196.2:c.249A>C	NP_671729.2:p.Pro83=
XM_006713097.2:c.90A>C	XP_006713160.1:p.Pro30=
XM_011533574.1:c.90A>C	XP_011531876.1:p.Pro30=
XM_006713097.4:c.90A>C	XP_006713160.1:p.Pro30=
XM_024453446.1:c.90A>C	XP_024309214.1:p.Pro30=
NM_001370524.1:c.90A>C	NP_001357453.1:p.Pro30=
NM_001370525.1:c.90A>C	NP_001357454.1:p.Pro30=
NM_147196.3:c.249A>C MANE Select	NP_671729.2:p.Pro83=