Canonical Allele Identifier: CA2320766544
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7123024G= , CM000681.2:g.7123024G= GRCh38
NC_000019.9:g.7123035G= , CM000681.1:g.7123035G= GRCh37
NC_000019.8:g.7074035G= NCBI36
NG_008852.2:g.175977C=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3259-35C= MANE Select ENSP00000303830.4:n.3259-35C=
ENST00000302850.9:c.3259-35C= ENSP00000303830.4:n.3259-35C=
ENST00000341500.9:c.3223-35C= ENSP00000342838.4:n.3223-35C=
ENST00000593970.1:n.105-35C=
ENST00000601099.1:n.135C=
NM_000208.2:c.3259-35C= NP_000199.2:n.3259-35C=
NM_000208.3:c.3259-35C= NP_000199.2:n.3259-35C=
NM_001079817.1:c.3223-35C= NP_001073285.1:n.3223-35C=
NM_001079817.2:c.3223-35C= NP_001073285.1:n.3223-35C=
XM_011527988.1:c.3334-35C= XP_011526290.1:n.3334-35C=
XM_011527989.1:c.3298-35C= XP_011526291.1:n.3298-35C=
XM_011527988.2:c.3256-35C= XP_011526290.2:n.3256-35C=
XM_011527989.3:c.3220-35C= XP_011526291.2:n.3220-35C=
NM_000208.4:c.3259-35C= MANE Select NP_000199.2:n.3259-35C=
NM_001079817.3:c.3223-35C= NP_001073285.1:n.3223-35C=