Canonical Allele Identifier: CA388036934
Gene: THSD1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.52971654A>C (hg19) chr13:g.52397519A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.52397519A>C , CM000675.2:g.52397519A>C GRCh38
NC_000013.10:g.52971654A>C , CM000675.1:g.52971654A>C GRCh37
NC_000013.9:g.51869655A>C NCBI36
NG_047168.1:g.13976T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000258613.5:c.734T>G MANE Select ENSP00000258613.4:p.Val245Gly
ENST00000648254.1:c.734T>G ENSP00000497520.1:p.Val245Gly
ENST00000258613.4:c.734T>G ENSP00000258613.4:p.Val245Gly
ENST00000349258.8:c.734T>G ENSP00000340650.4:p.Val245Gly
NM_018676.3:c.734T>G NP_061146.1:p.Val245Gly
NM_199263.2:c.734T>G NP_954872.1:p.Val245Gly
NM_018676.4:c.734T>G MANE Select NP_061146.1:p.Val245Gly
NM_199263.3:c.734T>G NP_954872.1:p.Val245Gly
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