Canonical Allele Identifier: CA2320771059
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132185G= , CM000681.2:g.7132185G= GRCh38
NC_000019.9:g.7132196G= , CM000681.1:g.7132196G= GRCh37
NC_000019.8:g.7083196G= NCBI36
NG_008852.2:g.166816C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2815C= MANE Select ENSP00000303830.4:p.Pro939=
ENST00000302850.9:c.2815C= ENSP00000303830.4:p.Pro939=
ENST00000341500.9:c.2779C= ENSP00000342838.4:p.Pro927=
NM_000208.2:c.2815C= NP_000199.2:p.Pro939=
NM_000208.3:c.2815C= NP_000199.2:p.Pro939=
NM_001079817.1:c.2779C= NP_001073285.1:p.Pro927=
NM_001079817.2:c.2779C= NP_001073285.1:p.Pro927=
XM_011527988.1:c.2893C= XP_011526290.1:p.Pro965=
XM_011527989.1:c.2857C= XP_011526291.1:p.Pro953=
XM_011527988.2:c.2815C= XP_011526290.2:p.Pro939=
XM_011527989.3:c.2779C= XP_011526291.2:p.Pro927=
NM_000208.4:c.2815C= MANE Select NP_000199.2:p.Pro939=
NM_001079817.3:c.2779C= NP_001073285.1:p.Pro927=