Canonical Allele Identifier: CA2320763770
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117316T= , CM000681.2:g.7117316T= GRCh38
NC_000019.9:g.7117327T= , CM000681.1:g.7117327T= GRCh37
NC_000019.8:g.7068327T= NCBI36
NG_008852.2:g.181685A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3889A= MANE Select ENSP00000303830.4:p.Ser1297=
ENST00000302850.9:c.3889A= ENSP00000303830.4:p.Ser1297=
ENST00000341500.9:c.3853A= ENSP00000342838.4:p.Ser1285=
NM_000208.2:c.3889A= NP_000199.2:p.Ser1297=
NM_000208.3:c.3889A= NP_000199.2:p.Ser1297=
NM_001079817.1:c.3853A= NP_001073285.1:p.Ser1285=
NM_001079817.2:c.3853A= NP_001073285.1:p.Ser1285=
XM_011527988.1:c.3964A= XP_011526290.1:p.Ser1322=
XM_011527989.1:c.3928A= XP_011526291.1:p.Ser1310=
XM_011527988.2:c.3886A= XP_011526290.2:p.Ser1296=
XM_011527989.3:c.3850A= XP_011526291.2:p.Ser1284=
NM_000208.4:c.3889A= MANE Select NP_000199.2:p.Ser1297=
NM_001079817.3:c.3853A= NP_001073285.1:p.Ser1285=