Canonical Allele Identifier: CA391670853

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.39591205C>G , CM000677.2:g.39591205C>G GRCh38
NC_000015.9:g.39883406C>G , CM000677.1:g.39883406C>G GRCh37
NC_000015.8:g.37670698C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003246.4:c.2268C>G (THBS1) MANE Select NP_003237.2:p.Phe756Leu
ENST00000260356.6:c.2268C>G (THBS1) MANE Select ENSP00000260356.5:p.Phe756Leu
NM_003246.2:c.2268C>G (THBS1) NP_003237.2:p.Phe756Leu
NM_003246.3:c.2268C>G (THBS1) NP_003237.2:p.Phe756Leu
ENST00000260356.5:c.2268C>G (THBS1) ENSP00000260356.5:p.Phe756Leu
ENST00000560894.1:n.278C>G (THBS1)
ENST00000642527.1:c.771-2631G>C (FSIP1)
XM_011521970.1:c.2268C>G (THBS1) XP_011520272.1:p.Phe756Leu
XM_011521971.1:c.2094C>G (THBS1) XP_011520273.1:p.Phe698Leu
XM_011521971.2:c.2094C>G (THBS1) XP_011520273.1:p.Phe698Leu
XR_931897.1:n.2516C>G (THBS1)