Canonical Allele Identifier: CA2320763736
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117275C= , CM000681.2:g.7117275C= GRCh38
NC_000019.9:g.7117286C= , CM000681.1:g.7117286C= GRCh37
NC_000019.8:g.7068286C= NCBI36
NG_008852.2:g.181726G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3930G= MANE Select ENSP00000303830.4:p.Lys1310=
ENST00000302850.9:c.3930G= ENSP00000303830.4:p.Lys1310=
ENST00000341500.9:c.3894G= ENSP00000342838.4:p.Lys1298=
NM_000208.2:c.3930G= NP_000199.2:p.Lys1310=
NM_000208.3:c.3930G= NP_000199.2:p.Lys1310=
NM_001079817.1:c.3894G= NP_001073285.1:p.Lys1298=
NM_001079817.2:c.3894G= NP_001073285.1:p.Lys1298=
XM_011527988.1:c.4005G= XP_011526290.1:p.Lys1335=
XM_011527989.1:c.3969G= XP_011526291.1:p.Lys1323=
XM_011527988.2:c.3927G= XP_011526290.2:p.Lys1309=
XM_011527989.3:c.3891G= XP_011526291.2:p.Lys1297=
NM_000208.4:c.3930G= MANE Select NP_000199.2:p.Lys1310=
NM_001079817.3:c.3894G= NP_001073285.1:p.Lys1298=