Canonical Allele Identifier: CA1329042691
Gene: IHH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.219060419_219060425delinsACAGGAC , CM000664.2:g.219060419_219060425delinsACAGGAC GRCh38
NC_000002.11:g.219925141_219925147delinsACAGGAC , CM000664.1:g.219925141_219925147delinsACAGGAC GRCh37
NC_000002.10:g.219633385_219633391delinsACAGGAC NCBI36
NG_016741.1:g.5092_5098delinsGTCCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000295731.7:c.43_49delinsGTCCTGT MANE Select ENSP00000295731.5:p.Val15=
ENST00000295731.6:c.43_49delinsGTCCTGT ENSP00000295731.5:p.Val15=
NM_002181.3:c.43_49delinsGTCCTGT NP_002172.2:p.Val15=
NM_002181.4:c.43_49delinsGTCCTGT MANE Select NP_002172.2:p.Val15=
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