Canonical Allele Identifier: CA6992221
Gene: THSD1 HGNC NCBI

Linked Data

dbSNP Id: rs776491275

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397918G>A , CM000675.2:g.52397918G>A GRCh38
NC_000013.10:g.52972053G>A , CM000675.1:g.52972053G>A GRCh37
NC_000013.9:g.51870054G>A NCBI36
NG_047168.1:g.13577C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.335C>T MANE Select ENSP00000258613.4:p.Thr112Ile
ENST00000648254.1:c.335C>T ENSP00000497520.1:p.Thr112Ile
ENST00000258613.4:c.335C>T ENSP00000258613.4:p.Thr112Ile
ENST00000349258.8:c.335C>T ENSP00000340650.4:p.Thr112Ile
NM_018676.3:c.335C>T NP_061146.1:p.Thr112Ile
NM_199263.2:c.335C>T NP_954872.1:p.Thr112Ile
NM_018676.4:c.335C>T MANE Select NP_061146.1:p.Thr112Ile
NM_199263.3:c.335C>T NP_954872.1:p.Thr112Ile