Canonical Allele Identifier: CA1474474593
Gene: IBSP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.87811453_87811456delinsAAGC , CM000666.2:g.87811453_87811456delinsAAGC GRCh38
NC_000004.11:g.88732605_88732608delinsAAGC , CM000666.1:g.88732605_88732608delinsAAGC GRCh37
NC_000004.10:g.88951629_88951632delinsAAGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000226284.7:c.497_500delinsAAGC MANE Select ENSP00000226284.5:p.Glu166=
ENST00000226284.6:c.497_500delinsAAGC ENSP00000226284.5:p.Glu166=
NM_004967.3:c.497_500delinsAAGC NP_004958.2:p.Glu166=
NM_004967.4:c.497_500delinsAAGC MANE Select NP_004958.2:p.Glu166=
Search 100 bp 5'
Search 100 bp 3'