Canonical Allele Identifier: CA402785129
Community Standard Title: NM_001308210.2(TSHZ1):c.2127C>A (p.Asp709Glu)
Gene: TSHZ1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.75287534C>A , CM000680.2:g.75287534C>A GRCh38
NC_000018.9:g.72999489C>A , CM000680.1:g.72999489C>A GRCh37
NC_000018.8:g.71128477C>A NCBI36
NG_032047.1:g.81780C>A

Transcript Alleles

HGVS Amino-acid Change
NM_001308210.2:c.2127C>A MANE Select NP_001295139.1:p.Asp709Glu
ENST00000580243.3:c.2127C>A MANE Select ENSP00000464391.1:p.Asp709Glu
NM_001308210.1:c.2127C>A NP_001295139.1:p.Asp709Glu
NM_005786.5:c.1992C>A NP_005777.3:p.Asp664Glu
NM_005786.6:c.1992C>A NP_005777.3:p.Asp664Glu
ENST00000322038.5:c.1992C>A ENSP00000323584.5:p.Asp664Glu
ENST00000580243.1:c.2127C>A ENSP00000464391.1:p.Asp709Glu
ENST00000584217.1:n.4671C>A
XM_005266641.2:c.1992C>A XP_005266698.1:p.Asp664Glu
XM_005266641.3:c.1992C>A XP_005266698.1:p.Asp664Glu