Canonical Allele Identifier: CA1558183720
Gene: THBS4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80065419A= , CM000667.2:g.80065419A= GRCh38
NC_000005.9:g.79361242A= , CM000667.1:g.79361242A= GRCh37
NC_000005.8:g.79396998A= NCBI36
NG_047084.1:g.79109A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350881.6:c.1136A= MANE Select ENSP00000339730.2:p.Asp379=
ENST00000511733.1:c.863A= ENSP00000422298.1:p.Asp288=
NM_001306212.1:c.863A= NP_001293141.1:p.Asp288=
NM_001306213.1:c.863A= NP_001293142.1:p.Asp288=
NM_001306214.1:c.863A= NP_001293143.1:p.Asp288=
NM_003248.4:c.1136A= NP_003239.2:p.Asp379=
NM_003248.5:c.1136A= NP_003239.2:p.Asp379=
XM_017009798.2:c.1136A= XP_016865287.1:p.Asp379=
XM_017009799.2:c.1136A= XP_016865288.1:p.Asp379=
XR_002956176.1:n.1327A=
NM_003248.6:c.1136A= MANE Select NP_003239.2:p.Asp379=
NM_001306212.2:c.863A= NP_001293141.1:p.Asp288=
NM_001306213.2:c.863A= NP_001293142.1:p.Asp288=
NM_001306214.2:c.863A= NP_001293143.1:p.Asp288=