Canonical Allele Identifier: CA2320765528
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7120688C= , CM000681.2:g.7120688C= GRCh38
NC_000019.9:g.7120699C= , CM000681.1:g.7120699C= GRCh37
NC_000019.8:g.7071699C= NCBI36
NG_008852.2:g.178313G=

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.3591G= MANE Select ENSP00000303830.4:p.Leu1197=
ENST00000302850.9:c.3591G= ENSP00000303830.4:p.Leu1197=
ENST00000341500.9:c.3555G= ENSP00000342838.4:p.Leu1185=
ENST00000601099.1:n.502G=
NM_000208.2:c.3591G= NP_000199.2:p.Leu1197=
NM_000208.3:c.3591G= NP_000199.2:p.Leu1197=
NM_001079817.1:c.3555G= NP_001073285.1:p.Leu1185=
NM_001079817.2:c.3555G= NP_001073285.1:p.Leu1185=
XM_011527988.1:c.3666G= XP_011526290.1:p.Leu1222=
XM_011527989.1:c.3630G= XP_011526291.1:p.Leu1210=
XM_011527988.2:c.3588G= XP_011526290.2:p.Leu1196=
XM_011527989.3:c.3552G= XP_011526291.2:p.Leu1184=
NM_000208.4:c.3591G= MANE Select NP_000199.2:p.Leu1197=
NM_001079817.3:c.3555G= NP_001073285.1:p.Leu1185=