Canonical Allele Identifier: CA403672224
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs1972806776

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132315C>G , CM000681.2:g.7132315C>G GRCh38
NC_000019.9:g.7132326C>G , CM000681.1:g.7132326C>G GRCh37
NC_000019.8:g.7083326C>G NCBI36
NG_008852.2:g.166686G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2685G>C MANE Select ENSP00000303830.4:p.Glu895Asp
ENST00000302850.9:c.2685G>C ENSP00000303830.4:p.Glu895Asp
ENST00000341500.9:c.2649G>C ENSP00000342838.4:p.Glu883Asp
NM_000208.2:c.2685G>C NP_000199.2:p.Glu895Asp
NM_000208.3:c.2685G>C NP_000199.2:p.Glu895Asp
NM_001079817.1:c.2649G>C NP_001073285.1:p.Glu883Asp
NM_001079817.2:c.2649G>C NP_001073285.1:p.Glu883Asp
XM_011527988.1:c.2763G>C XP_011526290.1:p.Glu921Asp
XM_011527989.1:c.2727G>C XP_011526291.1:p.Glu909Asp
XM_011527988.2:c.2685G>C XP_011526290.2:p.Glu895Asp
XM_011527989.3:c.2649G>C XP_011526291.2:p.Glu883Asp
NM_000208.4:c.2685G>C MANE Select NP_000199.2:p.Glu895Asp
NM_001079817.3:c.2649G>C NP_001073285.1:p.Glu883Asp