Canonical Allele Identifier: CA2320766458
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7122840T= , CM000681.2:g.7122840T= GRCh38
NC_000019.9:g.7122851T= , CM000681.1:g.7122851T= GRCh37
NC_000019.8:g.7073851T= NCBI36
NG_008852.2:g.176161A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3369+39A= MANE Select ENSP00000303830.4:n.3369+39A=
ENST00000302850.9:c.3369+39A= ENSP00000303830.4:n.3369+39A=
ENST00000341500.9:c.3333+39A= ENSP00000342838.4:n.3333+39A=
ENST00000593970.1:n.215+39A=
ENST00000601099.1:n.280+39A=
NM_000208.2:c.3369+39A= NP_000199.2:n.3369+39A=
NM_000208.3:c.3369+39A= NP_000199.2:n.3369+39A=
NM_001079817.1:c.3333+39A= NP_001073285.1:n.3333+39A=
NM_001079817.2:c.3333+39A= NP_001073285.1:n.3333+39A=
XM_011527988.1:c.3444+39A= XP_011526290.1:n.3444+39A=
XM_011527989.1:c.3408+39A= XP_011526291.1:n.3408+39A=
XM_011527988.2:c.3366+39A= XP_011526290.2:n.3366+39A=
XM_011527989.3:c.3330+39A= XP_011526291.2:n.3330+39A=
NM_000208.4:c.3369+39A= MANE Select NP_000199.2:n.3369+39A=
NM_001079817.3:c.3333+39A= NP_001073285.1:n.3333+39A=