Canonical Allele Identifier: CA2389526141
Gene: IGSF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.39777593_39777594delinsCT , CM000683.2:g.39777593_39777594delinsCT GRCh38
NC_000021.8:g.41149520_41149521delinsCT , CM000683.1:g.41149520_41149521delinsCT GRCh37
NC_000021.7:g.40071390_40071391delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380588.5:c.719-1497_719-1496delinsCT MANE Select ENSP00000369962.4:n.719-1497_719-1496delinsCT
ENST00000380588.4:c.719-1497_719-1496delinsCT ENSP00000369962.4:n.719-1497_719-1496delinsCT
ENST00000479378.1:n.825-1497_825-1496delinsCT
NM_001080444.1:c.719-1497_719-1496delinsCT NP_001073913.1:n.719-1497_719-1496delinsCT
XM_011529472.1:c.989-1497_989-1496delinsCT XP_011527774.1:n.989-1497_989-1496delinsCT
XM_011529473.1:c.989-1497_989-1496delinsCT XP_011527775.1:n.989-1497_989-1496delinsCT
XM_011529472.2:c.989-1497_989-1496delinsCT XP_011527774.1:n.989-1497_989-1496delinsCT
NM_001080444.2:c.719-1497_719-1496delinsCT MANE Select NP_001073913.1:n.719-1497_719-1496delinsCT