Canonical Allele Identifier: CA2320763702
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117206C= , CM000681.2:g.7117206C= GRCh38
NC_000019.9:g.7117217C= , CM000681.1:g.7117217C= GRCh37
NC_000019.8:g.7068217C= NCBI36
NG_008852.2:g.181795G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3999G= MANE Select ENSP00000303830.4:p.Ser1333=
ENST00000302850.9:c.3999G= ENSP00000303830.4:p.Ser1333=
ENST00000341500.9:c.3963G= ENSP00000342838.4:p.Ser1321=
NM_000208.2:c.3999G= NP_000199.2:p.Ser1333=
NM_000208.3:c.3999G= NP_000199.2:p.Ser1333=
NM_001079817.1:c.3963G= NP_001073285.1:p.Ser1321=
NM_001079817.2:c.3963G= NP_001073285.1:p.Ser1321=
XM_011527988.1:c.4074G= XP_011526290.1:p.Ser1358=
XM_011527989.1:c.4038G= XP_011526291.1:p.Ser1346=
XM_011527988.2:c.3996G= XP_011526290.2:p.Ser1332=
XM_011527989.3:c.3960G= XP_011526291.2:p.Ser1320=
NM_000208.4:c.3999G= MANE Select NP_000199.2:p.Ser1333=
NM_001079817.3:c.3963G= NP_001073285.1:p.Ser1321=