Canonical Allele Identifier: CA352480541

Gene: TMIE

Linked Data

• MyVariant Identifiers: chr3:g.46750640A>T (hg19) ; chr3:g.46709150A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.46709150A>T , CM000665.2:g.46709150A>T	GRCh38
NC_000003.11:g.46750640A>T , CM000665.1:g.46750640A>T	GRCh37
NC_000003.10:g.46725644A>T	NCBI36
NG_011628.1:g.12818A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000643606.3:c.236A>T MANE Select	ENSP00000494576.2:p.Asn79Ile
ENST00000644830.1:c.77A>T	ENSP00000495111.1:p.Asn26Ile
ENST00000651652.1:c.134A>T	ENSP00000498953.1:p.Asn45Ile
ENST00000326431.3:c.236A>T	ENSP00000324775.3:p.Asn79Ile
NM_147196.2:c.236A>T	NP_671729.2:p.Asn79Ile
XM_006713097.2:c.77A>T	XP_006713160.1:p.Asn26Ile
XM_011533574.1:c.77A>T	XP_011531876.1:p.Asn26Ile
XM_006713097.4:c.77A>T	XP_006713160.1:p.Asn26Ile
XM_024453446.1:c.77A>T	XP_024309214.1:p.Asn26Ile
NM_001370524.1:c.77A>T	NP_001357453.1:p.Asn26Ile
NM_001370525.1:c.77A>T	NP_001357454.1:p.Asn26Ile
NM_147196.3:c.236A>T MANE Select	NP_671729.2:p.Asn79Ile