Canonical Allele Identifier: CA2320763706
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117211A= , CM000681.2:g.7117211A= GRCh38
NC_000019.9:g.7117222A= , CM000681.1:g.7117222A= GRCh37
NC_000019.8:g.7068222A= NCBI36
NG_008852.2:g.181790T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3994T= MANE Select ENSP00000303830.4:p.Ser1332=
ENST00000302850.9:c.3994T= ENSP00000303830.4:p.Ser1332=
ENST00000341500.9:c.3958T= ENSP00000342838.4:p.Ser1320=
NM_000208.2:c.3994T= NP_000199.2:p.Ser1332=
NM_000208.3:c.3994T= NP_000199.2:p.Ser1332=
NM_001079817.1:c.3958T= NP_001073285.1:p.Ser1320=
NM_001079817.2:c.3958T= NP_001073285.1:p.Ser1320=
XM_011527988.1:c.4069T= XP_011526290.1:p.Ser1357=
XM_011527989.1:c.4033T= XP_011526291.1:p.Ser1345=
XM_011527988.2:c.3991T= XP_011526290.2:p.Ser1331=
XM_011527989.3:c.3955T= XP_011526291.2:p.Ser1319=
NM_000208.4:c.3994T= MANE Select NP_000199.2:p.Ser1332=
NM_001079817.3:c.3958T= NP_001073285.1:p.Ser1320=