Canonical Allele Identifier: CA1425864403
Gene: HTR3E HGNC NCBI
HTR3E-AS1 HGNC NCBI
EIF2B5-DT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184100628G= , CM000665.2:g.184100628G= GRCh38
NC_000003.11:g.183818416G= , CM000665.1:g.183818416G= GRCh37
NC_000003.10:g.185301110G= NCBI36
NG_012452.1:g.5450G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000335304.6:c.256G= (HTR3E) ENSP00000335511.2:p.Ala86=
ENST00000415389.6:c.211G= (HTR3E) MANE Select ENSP00000401444.2:p.Ala71=
ENST00000425359.6:c.211G= (HTR3E) ENSP00000401900.2:p.Ala71=
ENST00000431041.5:c.-3G= (HTR3E) ENSP00000391254.1:n.-3G=
ENST00000436361.6:c.256G= (HTR3E) ENSP00000395833.2:p.Ala86=
ENST00000440596.2:c.256G= (HTR3E) ENSP00000406050.2:p.Ala86=
NM_001256613.1:c.211G= (HTR3E) NP_001243542.1:p.Ala71=
NM_001256614.1:c.256G= (HTR3E) NP_001243543.1:p.Ala86=
NM_182589.2:c.256G= (HTR3E) NP_872395.2:p.Ala86=
NM_198313.2:c.211G= (HTR3E) NP_938055.1:p.Ala71=
NM_198314.2:c.256G= (HTR3E) NP_938056.1:p.Ala86=
NR_133658.1:n.282+3532C= (HTR3E-AS1)
XR_002959683.1:n.671-26541C= (EIF2B5-DT)
NM_001256613.2:c.211G= (HTR3E) MANE Select NP_001243542.1:p.Ala71=
NM_198313.3:c.211G= (HTR3E) NP_938055.1:p.Ala71=