Canonical Allele Identifier: CA2320766555
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7123045G= , CM000681.2:g.7123045G= GRCh38
NC_000019.9:g.7123056G= , CM000681.1:g.7123056G= GRCh37
NC_000019.8:g.7074056G= NCBI36
NG_008852.2:g.175956C=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3259-56C= MANE Select ENSP00000303830.4:n.3259-56C=
ENST00000302850.9:c.3259-56C= ENSP00000303830.4:n.3259-56C=
ENST00000341500.9:c.3223-56C= ENSP00000342838.4:n.3223-56C=
ENST00000593970.1:n.105-56C=
ENST00000601099.1:n.114C=
NM_000208.2:c.3259-56C= NP_000199.2:n.3259-56C=
NM_000208.3:c.3259-56C= NP_000199.2:n.3259-56C=
NM_001079817.1:c.3223-56C= NP_001073285.1:n.3223-56C=
NM_001079817.2:c.3223-56C= NP_001073285.1:n.3223-56C=
XM_011527988.1:c.3334-56C= XP_011526290.1:n.3334-56C=
XM_011527989.1:c.3298-56C= XP_011526291.1:n.3298-56C=
XM_011527988.2:c.3256-56C= XP_011526290.2:n.3256-56C=
XM_011527989.3:c.3220-56C= XP_011526291.2:n.3220-56C=
NM_000208.4:c.3259-56C= MANE Select NP_000199.2:n.3259-56C=
NM_001079817.3:c.3223-56C= NP_001073285.1:n.3223-56C=