Canonical Allele Identifier: CA2320790741
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7172395A= , CM000681.2:g.7172395A= GRCh38
NC_000019.9:g.7172406A= , CM000681.1:g.7172406A= GRCh37
NC_000019.8:g.7123406A= NCBI36
NG_008852.2:g.126606T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.1163T= MANE Select ENSP00000303830.4:p.Ile388=
ENST00000302850.9:c.1163T= ENSP00000303830.4:p.Ile388=
ENST00000341500.9:c.1163T= ENSP00000342838.4:p.Ile388=
ENST00000598216.1:n.1138T=
NM_000208.2:c.1163T= NP_000199.2:p.Ile388=
NM_000208.3:c.1163T= NP_000199.2:p.Ile388=
NM_001079817.1:c.1163T= NP_001073285.1:p.Ile388=
NM_001079817.2:c.1163T= NP_001073285.1:p.Ile388=
XM_011527988.1:c.1241T= XP_011526290.1:p.Ile414=
XM_011527989.1:c.1241T= XP_011526291.1:p.Ile414=
XM_011527988.2:c.1163T= XP_011526290.2:p.Ile388=
XM_011527989.3:c.1163T= XP_011526291.2:p.Ile388=
NM_000208.4:c.1163T= MANE Select NP_000199.2:p.Ile388=
NM_001079817.3:c.1163T= NP_001073285.1:p.Ile388=