Canonical Allele Identifier: CA403672189
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132299A>G , CM000681.2:g.7132299A>G GRCh38
NC_000019.9:g.7132310A>G , CM000681.1:g.7132310A>G GRCh37
NC_000019.8:g.7083310A>G NCBI36
NG_008852.2:g.166702T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2701T>C MANE Select ENSP00000303830.4:p.Ser901Pro
ENST00000302850.9:c.2701T>C ENSP00000303830.4:p.Ser901Pro
ENST00000341500.9:c.2665T>C ENSP00000342838.4:p.Ser889Pro
NM_000208.2:c.2701T>C NP_000199.2:p.Ser901Pro
NM_000208.3:c.2701T>C NP_000199.2:p.Ser901Pro
NM_001079817.1:c.2665T>C NP_001073285.1:p.Ser889Pro
NM_001079817.2:c.2665T>C NP_001073285.1:p.Ser889Pro
XM_011527988.1:c.2779T>C XP_011526290.1:p.Ser927Pro
XM_011527989.1:c.2743T>C XP_011526291.1:p.Ser915Pro
XM_011527988.2:c.2701T>C XP_011526290.2:p.Ser901Pro
XM_011527989.3:c.2665T>C XP_011526291.2:p.Ser889Pro
NM_000208.4:c.2701T>C MANE Select NP_000199.2:p.Ser901Pro
NM_001079817.3:c.2665T>C NP_001073285.1:p.Ser889Pro