Canonical Allele Identifier: CA2320796137
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7184383G= , CM000681.2:g.7184383G= GRCh38
NC_000019.9:g.7184394G= , CM000681.1:g.7184394G= GRCh37
NC_000019.8:g.7135394G= NCBI36
NG_008852.2:g.114618C=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.907C= MANE Select ENSP00000303830.4:p.Gln303=
ENST00000302850.9:c.907C= ENSP00000303830.4:p.Gln303=
ENST00000341500.9:c.907C= ENSP00000342838.4:p.Gln303=
ENST00000598216.1:n.882C=
NM_000208.2:c.907C= NP_000199.2:p.Gln303=
NM_000208.3:c.907C= NP_000199.2:p.Gln303=
NM_001079817.1:c.907C= NP_001073285.1:p.Gln303=
NM_001079817.2:c.907C= NP_001073285.1:p.Gln303=
XM_011527988.1:c.985C= XP_011526290.1:p.Gln329=
XM_011527989.1:c.985C= XP_011526291.1:p.Gln329=
XM_011527988.2:c.907C= XP_011526290.2:p.Gln303=
XM_011527989.3:c.907C= XP_011526291.2:p.Gln303=
NM_000208.4:c.907C= MANE Select NP_000199.2:p.Gln303=
NM_001079817.3:c.907C= NP_001073285.1:p.Gln303=