Canonical Allele Identifier: CA2320776197
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7142972T= , CM000681.2:g.7142972T= GRCh38
NC_000019.9:g.7142983T= , CM000681.1:g.7142983T= GRCh37
NC_000019.8:g.7093983T= NCBI36
NG_008852.2:g.156029A=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.2386A= MANE Select ENSP00000303830.4:p.Arg796=
ENST00000302850.9:c.2386A= ENSP00000303830.4:p.Arg796=
ENST00000341500.9:c.2350A= ENSP00000342838.4:p.Arg784=
ENST00000597211.1:n.69A=
NM_000208.2:c.2386A= NP_000199.2:p.Arg796=
NM_000208.3:c.2386A= NP_000199.2:p.Arg796=
NM_001079817.1:c.2350A= NP_001073285.1:p.Arg784=
NM_001079817.2:c.2350A= NP_001073285.1:p.Arg784=
XM_011527988.1:c.2464A= XP_011526290.1:p.Arg822=
XM_011527989.1:c.2428A= XP_011526291.1:p.Arg810=
XM_011527988.2:c.2386A= XP_011526290.2:p.Arg796=
XM_011527989.3:c.2350A= XP_011526291.2:p.Arg784=
NM_000208.4:c.2386A= MANE Select NP_000199.2:p.Arg796=
NM_001079817.3:c.2350A= NP_001073285.1:p.Arg784=