Canonical Allele Identifier: CA2320767923
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125338C= , CM000681.2:g.7125338C= GRCh38
NC_000019.9:g.7125349C= , CM000681.1:g.7125349C= GRCh37
NC_000019.8:g.7076349C= NCBI36
NG_008852.2:g.173663G=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3203G= MANE Select ENSP00000303830.4:p.Arg1068=
ENST00000302850.9:c.3203G= ENSP00000303830.4:p.Arg1068=
ENST00000341500.9:c.3167G= ENSP00000342838.4:p.Arg1056=
ENST00000593970.1:n.49G=
NM_000208.2:c.3203G= NP_000199.2:p.Arg1068=
NM_000208.3:c.3203G= NP_000199.2:p.Arg1068=
NM_001079817.1:c.3167G= NP_001073285.1:p.Arg1056=
NM_001079817.2:c.3167G= NP_001073285.1:p.Arg1056=
XM_011527988.1:c.3278G= XP_011526290.1:p.Arg1093=
XM_011527989.1:c.3242G= XP_011526291.1:p.Arg1081=
XM_011527988.2:c.3200G= XP_011526290.2:p.Arg1067=
XM_011527989.3:c.3164G= XP_011526291.2:p.Arg1055=
NM_000208.4:c.3203G= MANE Select NP_000199.2:p.Arg1068=
NM_001079817.3:c.3167G= NP_001073285.1:p.Arg1056=