Canonical Allele Identifier: CA2320776139
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7143082C= , CM000681.2:g.7143082C= GRCh38
NC_000019.9:g.7143093C= , CM000681.1:g.7143093C= GRCh37
NC_000019.8:g.7094093C= NCBI36
NG_008852.2:g.155919G=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.2276G= MANE Select ENSP00000303830.4:p.Arg759=
ENST00000302850.9:c.2276G= ENSP00000303830.4:p.Arg759=
ENST00000341500.9:c.2240G= ENSP00000342838.4:p.Arg747=
NM_000208.2:c.2276G= NP_000199.2:p.Arg759=
NM_000208.3:c.2276G= NP_000199.2:p.Arg759=
NM_001079817.1:c.2240G= NP_001073285.1:p.Arg747=
NM_001079817.2:c.2240G= NP_001073285.1:p.Arg747=
XM_011527988.1:c.2354G= XP_011526290.1:p.Arg785=
XM_011527989.1:c.2318G= XP_011526291.1:p.Arg773=
XM_011527988.2:c.2276G= XP_011526290.2:p.Arg759=
XM_011527989.3:c.2240G= XP_011526291.2:p.Arg747=
NM_000208.4:c.2276G= MANE Select NP_000199.2:p.Arg759=
NM_001079817.3:c.2240G= NP_001073285.1:p.Arg747=