Canonical Allele Identifier: CA2320763876
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117030G= , CM000681.2:g.7117030G= GRCh38
NC_000019.9:g.7117041G= , CM000681.1:g.7117041G= GRCh37
NC_000019.8:g.7068041G= NCBI36
NG_008852.2:g.181971C=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*26C= MANE Select ENSP00000303830.4:n.*26C=
ENST00000302850.9:c.*26C= ENSP00000303830.4:n.*26C=
ENST00000341500.9:c.*26C= ENSP00000342838.4:n.*26C=
NM_000208.2:c.*26C= NP_000199.2:n.*26C=
NM_000208.3:c.*26C= NP_000199.2:n.*26C=
NM_001079817.1:c.*26C= NP_001073285.1:n.*26C=
NM_001079817.2:c.*26C= NP_001073285.1:n.*26C=
XM_011527988.1:c.*26C= XP_011526290.1:n.*26C=
XM_011527989.1:c.*26C= XP_011526291.1:n.*26C=
XM_011527988.2:c.*26C= XP_011526290.2:n.*26C=
XM_011527989.3:c.*26C= XP_011526291.2:n.*26C=
NM_000208.4:c.*26C= MANE Select NP_000199.2:n.*26C=
NM_001079817.3:c.*26C= NP_001073285.1:n.*26C=