Canonical Allele Identifier: CA2830535184
Gene: FSTL5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.161542657_161542658insAGAG , CM000666.2:g.161542657_161542658insAGAG GRCh38
NC_000004.11:g.162463809_162463810insAGAG , CM000666.1:g.162463809_162463810insAGAG GRCh37
NC_000004.10:g.162683259_162683260insAGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000306100.10:c.1053_1054insCTCT MANE Select ENSP00000305334.4:p.Arg352LeufsTer2
ENST00000306100.9:c.1053_1054insCTCT ENSP00000305334.4:p.Arg352LeufsTer2
ENST00000379164.8:c.1050_1051insCTCT ENSP00000368462.4:p.Arg351LeufsTer2
ENST00000427802.2:c.1050_1051insCTCT ENSP00000389270.2:p.Arg351LeufsTer2
ENST00000511170.1:n.505_506insCTCT
NM_001128427.2:c.1050_1051insCTCT NP_001121899.1:p.Arg351LeufsTer2
NM_001128428.2:c.1050_1051insCTCT NP_001121900.1:p.Arg351LeufsTer2
NM_020116.4:c.1053_1054insCTCT NP_064501.2:p.Arg352LeufsTer2
XM_011532126.1:c.1053_1054insCTCT XP_011530428.1:p.Arg352LeufsTer2
NM_020116.5:c.1053_1054insCTCT MANE Select NP_064501.2:p.Arg352LeufsTer2
NM_001128427.3:c.1050_1051insCTCT NP_001121899.1:p.Arg351LeufsTer2
NM_001128428.3:c.1050_1051insCTCT NP_001121900.1:p.Arg351LeufsTer2