Canonical Allele Identifier: CA1362233128

Gene: TMIE

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46705857T= , CM000665.2:g.46705857T=	GRCh38
NC_000003.11:g.46747347T= , CM000665.1:g.46747347T=	GRCh37
NC_000003.10:g.46722351T=	NCBI36
NG_011628.1:g.9525T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.161T= MANE Select	ENSP00000494576.2:p.Met54=
ENST00000644830.1:c.2T=	ENSP00000495111.1:p.Met1=
ENST00000651652.1:c.59T=	ENSP00000498953.1:p.Met20=
ENST00000326431.3:c.161T=	ENSP00000324775.3:p.Met54=
NM_147196.2:c.161T=	NP_671729.2:p.Met54=
XM_006713097.2:c.2T=	XP_006713160.1:p.Met1=
XM_011533574.1:c.2T=	XP_011531876.1:p.Met1=
XM_006713097.4:c.2T=	XP_006713160.1:p.Met1=
XM_024453446.1:c.2T=	XP_024309214.1:p.Met1=
NM_001370524.1:c.2T=	NP_001357453.1:p.Met1=
NM_001370525.1:c.2T=	NP_001357454.1:p.Met1=
NM_147196.3:c.161T= MANE Select	NP_671729.2:p.Met54=