Canonical Allele Identifier: CA2830535185
Gene: FSTL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.161542661_161542662insGGG , CM000666.2:g.161542661_161542662insGGG GRCh38
NC_000004.11:g.162463813_162463814insGGG , CM000666.1:g.162463813_162463814insGGG GRCh37
NC_000004.10:g.162683263_162683264insGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306100.10:c.1048_1049insCCC MANE Select ENSP00000305334.4:p.Ser349_Gln350insPro
ENST00000306100.9:c.1048_1049insCCC ENSP00000305334.4:p.Ser349_Gln350insPro
ENST00000379164.8:c.1045_1046insCCC ENSP00000368462.4:p.Ser348_Gln349insPro
ENST00000427802.2:c.1045_1046insCCC ENSP00000389270.2:p.Ser348_Gln349insPro
ENST00000511170.1:n.500_501insCCC
NM_001128427.2:c.1045_1046insCCC NP_001121899.1:p.Ser348_Gln349insPro
NM_001128428.2:c.1045_1046insCCC NP_001121900.1:p.Ser348_Gln349insPro
NM_020116.4:c.1048_1049insCCC NP_064501.2:p.Ser349_Gln350insPro
XM_011532126.1:c.1048_1049insCCC XP_011530428.1:p.Ser349_Gln350insPro
NM_020116.5:c.1048_1049insCCC MANE Select NP_064501.2:p.Ser349_Gln350insPro
NM_001128427.3:c.1045_1046insCCC NP_001121899.1:p.Ser348_Gln349insPro
NM_001128428.3:c.1045_1046insCCC NP_001121900.1:p.Ser348_Gln349insPro