Canonical Allele Identifier: CA403672215
Gene: INSR HGNC NCBI

Linked Data

gnomAD v4: 19-7132311-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132311G>A , CM000681.2:g.7132311G>A GRCh38
NC_000019.9:g.7132322G>A , CM000681.1:g.7132322G>A GRCh37
NC_000019.8:g.7083322G>A NCBI36
NG_008852.2:g.166690C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2689C>T MANE Select ENSP00000303830.4:p.His897Tyr
ENST00000302850.9:c.2689C>T ENSP00000303830.4:p.His897Tyr
ENST00000341500.9:c.2653C>T ENSP00000342838.4:p.His885Tyr
NM_000208.2:c.2689C>T NP_000199.2:p.His897Tyr
NM_000208.3:c.2689C>T NP_000199.2:p.His897Tyr
NM_001079817.1:c.2653C>T NP_001073285.1:p.His885Tyr
NM_001079817.2:c.2653C>T NP_001073285.1:p.His885Tyr
XM_011527988.1:c.2767C>T XP_011526290.1:p.His923Tyr
XM_011527989.1:c.2731C>T XP_011526291.1:p.His911Tyr
XM_011527988.2:c.2689C>T XP_011526290.2:p.His897Tyr
XM_011527989.3:c.2653C>T XP_011526291.2:p.His885Tyr
NM_000208.4:c.2689C>T MANE Select NP_000199.2:p.His897Tyr
NM_001079817.3:c.2653C>T NP_001073285.1:p.His885Tyr