Canonical Allele Identifier: CA2389526147
Gene: IGSF5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.39777604_39777608delinsCTCTA , CM000683.2:g.39777604_39777608delinsCTCTA GRCh38
NC_000021.8:g.41149531_41149535delinsCTCTA , CM000683.1:g.41149531_41149535delinsCTCTA GRCh37
NC_000021.7:g.40071401_40071405delinsCTCTA NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000380588.5:c.719-1486_719-1482delinsCTCTA MANE Select ENSP00000369962.4:n.719-1486_719-1482delinsCTCTA
ENST00000380588.4:c.719-1486_719-1482delinsCTCTA ENSP00000369962.4:n.719-1486_719-1482delinsCTCTA
ENST00000479378.1:n.825-1486_825-1482delinsCTCTA
NM_001080444.1:c.719-1486_719-1482delinsCTCTA NP_001073913.1:n.719-1486_719-1482delinsCTCTA
XM_011529472.1:c.989-1486_989-1482delinsCTCTA XP_011527774.1:n.989-1486_989-1482delinsCTCTA
XM_011529473.1:c.989-1486_989-1482delinsCTCTA XP_011527775.1:n.989-1486_989-1482delinsCTCTA
XM_011529472.2:c.989-1486_989-1482delinsCTCTA XP_011527774.1:n.989-1486_989-1482delinsCTCTA
NM_001080444.2:c.719-1486_719-1482delinsCTCTA MANE Select NP_001073913.1:n.719-1486_719-1482delinsCTCTA