Canonical Allele Identifier: CA2320763693
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117183C= , CM000681.2:g.7117183C= GRCh38
NC_000019.9:g.7117194C= , CM000681.1:g.7117194C= GRCh37
NC_000019.8:g.7068194C= NCBI36
NG_008852.2:g.181818G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.4022G= MANE Select ENSP00000303830.4:p.Gly1341=
ENST00000302850.9:c.4022G= ENSP00000303830.4:p.Gly1341=
ENST00000341500.9:c.3986G= ENSP00000342838.4:p.Gly1329=
NM_000208.2:c.4022G= NP_000199.2:p.Gly1341=
NM_000208.3:c.4022G= NP_000199.2:p.Gly1341=
NM_001079817.1:c.3986G= NP_001073285.1:p.Gly1329=
NM_001079817.2:c.3986G= NP_001073285.1:p.Gly1329=
XM_011527988.1:c.4097G= XP_011526290.1:p.Gly1366=
XM_011527989.1:c.4061G= XP_011526291.1:p.Gly1354=
XM_011527988.2:c.4019G= XP_011526290.2:p.Gly1340=
XM_011527989.3:c.3983G= XP_011526291.2:p.Gly1328=
NM_000208.4:c.4022G= MANE Select NP_000199.2:p.Gly1341=
NM_001079817.3:c.3986G= NP_001073285.1:p.Gly1329=