Canonical Allele Identifier: CA2320763804
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117342T= , CM000681.2:g.7117342T= GRCh38
NC_000019.9:g.7117353T= , CM000681.1:g.7117353T= GRCh37
NC_000019.8:g.7068353T= NCBI36
NG_008852.2:g.181659A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3863A= MANE Select ENSP00000303830.4:p.Asn1288=
ENST00000302850.9:c.3863A= ENSP00000303830.4:p.Asn1288=
ENST00000341500.9:c.3827A= ENSP00000342838.4:p.Asn1276=
NM_000208.2:c.3863A= NP_000199.2:p.Asn1288=
NM_000208.3:c.3863A= NP_000199.2:p.Asn1288=
NM_001079817.1:c.3827A= NP_001073285.1:p.Asn1276=
NM_001079817.2:c.3827A= NP_001073285.1:p.Asn1276=
XM_011527988.1:c.3938A= XP_011526290.1:p.Asn1313=
XM_011527989.1:c.3902A= XP_011526291.1:p.Asn1301=
XM_011527988.2:c.3860A= XP_011526290.2:p.Asn1287=
XM_011527989.3:c.3824A= XP_011526291.2:p.Asn1275=
NM_000208.4:c.3863A= MANE Select NP_000199.2:p.Asn1288=
NM_001079817.3:c.3827A= NP_001073285.1:p.Asn1276=