Canonical Allele Identifier: CA403671133
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125360C>G , CM000681.2:g.7125360C>G GRCh38
NC_000019.9:g.7125371C>G , CM000681.1:g.7125371C>G GRCh37
NC_000019.8:g.7076371C>G NCBI36
NG_008852.2:g.173641G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3181G>C MANE Select ENSP00000303830.4:p.Glu1061Gln
ENST00000302850.9:c.3181G>C ENSP00000303830.4:p.Glu1061Gln
ENST00000341500.9:c.3145G>C ENSP00000342838.4:p.Glu1049Gln
ENST00000593970.1:n.27G>C
NM_000208.2:c.3181G>C NP_000199.2:p.Glu1061Gln
NM_000208.3:c.3181G>C NP_000199.2:p.Glu1061Gln
NM_001079817.1:c.3145G>C NP_001073285.1:p.Glu1049Gln
NM_001079817.2:c.3145G>C NP_001073285.1:p.Glu1049Gln
XM_011527988.1:c.3256G>C XP_011526290.1:p.Glu1086Gln
XM_011527989.1:c.3220G>C XP_011526291.1:p.Glu1074Gln
XM_011527988.2:c.3178G>C XP_011526290.2:p.Glu1060Gln
XM_011527989.3:c.3142G>C XP_011526291.2:p.Glu1048Gln
NM_000208.4:c.3181G>C MANE Select NP_000199.2:p.Glu1061Gln
NM_001079817.3:c.3145G>C NP_001073285.1:p.Glu1049Gln