Canonical Allele Identifier: CA403668794
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117327T>G , CM000681.2:g.7117327T>G GRCh38
NC_000019.9:g.7117338T>G , CM000681.1:g.7117338T>G GRCh37
NC_000019.8:g.7068338T>G NCBI36
NG_008852.2:g.181674A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3878A>C MANE Select ENSP00000303830.4:p.Asp1293Ala
ENST00000302850.9:c.3878A>C ENSP00000303830.4:p.Asp1293Ala
ENST00000341500.9:c.3842A>C ENSP00000342838.4:p.Asp1281Ala
NM_000208.2:c.3878A>C NP_000199.2:p.Asp1293Ala
NM_000208.3:c.3878A>C NP_000199.2:p.Asp1293Ala
NM_001079817.1:c.3842A>C NP_001073285.1:p.Asp1281Ala
NM_001079817.2:c.3842A>C NP_001073285.1:p.Asp1281Ala
XM_011527988.1:c.3953A>C XP_011526290.1:p.Asp1318Ala
XM_011527989.1:c.3917A>C XP_011526291.1:p.Asp1306Ala
XM_011527988.2:c.3875A>C XP_011526290.2:p.Asp1292Ala
XM_011527989.3:c.3839A>C XP_011526291.2:p.Asp1280Ala
NM_000208.4:c.3878A>C MANE Select NP_000199.2:p.Asp1293Ala
NM_001079817.3:c.3842A>C NP_001073285.1:p.Asp1281Ala