Canonical Allele Identifier: CA388036738
Gene: THSD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397425C>G , CM000675.2:g.52397425C>G GRCh38
NC_000013.10:g.52971560C>G , CM000675.1:g.52971560C>G GRCh37
NC_000013.9:g.51869561C>G NCBI36
NG_047168.1:g.14070G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.828G>C MANE Select ENSP00000258613.4:p.Lys276Asn
ENST00000648254.1:c.828G>C ENSP00000497520.1:p.Lys276Asn
ENST00000258613.4:c.828G>C ENSP00000258613.4:p.Lys276Asn
ENST00000349258.8:c.828G>C ENSP00000340650.4:p.Lys276Asn
NM_018676.3:c.828G>C NP_061146.1:p.Lys276Asn
NM_199263.2:c.828G>C NP_954872.1:p.Lys276Asn
NM_018676.4:c.828G>C MANE Select NP_061146.1:p.Lys276Asn
NM_199263.3:c.828G>C NP_954872.1:p.Lys276Asn