Canonical Allele Identifier: CA2320766545
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7123025T= , CM000681.2:g.7123025T= GRCh38
NC_000019.9:g.7123036T= , CM000681.1:g.7123036T= GRCh37
NC_000019.8:g.7074036T= NCBI36
NG_008852.2:g.175976A=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3259-36A= MANE Select ENSP00000303830.4:n.3259-36A=
ENST00000302850.9:c.3259-36A= ENSP00000303830.4:n.3259-36A=
ENST00000341500.9:c.3223-36A= ENSP00000342838.4:n.3223-36A=
ENST00000593970.1:n.105-36A=
ENST00000601099.1:n.134A=
NM_000208.2:c.3259-36A= NP_000199.2:n.3259-36A=
NM_000208.3:c.3259-36A= NP_000199.2:n.3259-36A=
NM_001079817.1:c.3223-36A= NP_001073285.1:n.3223-36A=
NM_001079817.2:c.3223-36A= NP_001073285.1:n.3223-36A=
XM_011527988.1:c.3334-36A= XP_011526290.1:n.3334-36A=
XM_011527989.1:c.3298-36A= XP_011526291.1:n.3298-36A=
XM_011527988.2:c.3256-36A= XP_011526290.2:n.3256-36A=
XM_011527989.3:c.3220-36A= XP_011526291.2:n.3220-36A=
NM_000208.4:c.3259-36A= MANE Select NP_000199.2:n.3259-36A=
NM_001079817.3:c.3223-36A= NP_001073285.1:n.3223-36A=