Canonical Allele Identifier: CA2320765526
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7120682A= , CM000681.2:g.7120682A= GRCh38
NC_000019.9:g.7120693A= , CM000681.1:g.7120693A= GRCh37
NC_000019.8:g.7071693A= NCBI36
NG_008852.2:g.178319T=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3597T= MANE Select ENSP00000303830.4:p.Pro1199=
ENST00000302850.9:c.3597T= ENSP00000303830.4:p.Pro1199=
ENST00000341500.9:c.3561T= ENSP00000342838.4:p.Pro1187=
ENST00000601099.1:n.508T=
NM_000208.2:c.3597T= NP_000199.2:p.Pro1199=
NM_000208.3:c.3597T= NP_000199.2:p.Pro1199=
NM_001079817.1:c.3561T= NP_001073285.1:p.Pro1187=
NM_001079817.2:c.3561T= NP_001073285.1:p.Pro1187=
XM_011527988.1:c.3672T= XP_011526290.1:p.Pro1224=
XM_011527989.1:c.3636T= XP_011526291.1:p.Pro1212=
XM_011527988.2:c.3594T= XP_011526290.2:p.Pro1198=
XM_011527989.3:c.3558T= XP_011526291.2:p.Pro1186=
NM_000208.4:c.3597T= MANE Select NP_000199.2:p.Pro1199=
NM_001079817.3:c.3561T= NP_001073285.1:p.Pro1187=