Canonical Allele Identifier: CA2320763705
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117210G= , CM000681.2:g.7117210G= GRCh38
NC_000019.9:g.7117221G= , CM000681.1:g.7117221G= GRCh37
NC_000019.8:g.7068221G= NCBI36
NG_008852.2:g.181791C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3995C= MANE Select ENSP00000303830.4:p.Ser1332=
ENST00000302850.9:c.3995C= ENSP00000303830.4:p.Ser1332=
ENST00000341500.9:c.3959C= ENSP00000342838.4:p.Ser1320=
NM_000208.2:c.3995C= NP_000199.2:p.Ser1332=
NM_000208.3:c.3995C= NP_000199.2:p.Ser1332=
NM_001079817.1:c.3959C= NP_001073285.1:p.Ser1320=
NM_001079817.2:c.3959C= NP_001073285.1:p.Ser1320=
XM_011527988.1:c.4070C= XP_011526290.1:p.Ser1357=
XM_011527989.1:c.4034C= XP_011526291.1:p.Ser1345=
XM_011527988.2:c.3992C= XP_011526290.2:p.Ser1331=
XM_011527989.3:c.3956C= XP_011526291.2:p.Ser1319=
NM_000208.4:c.3995C= MANE Select NP_000199.2:p.Ser1332=
NM_001079817.3:c.3959C= NP_001073285.1:p.Ser1320=