Canonical Allele Identifier: CA505217361
Gene: INSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7128870T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7128859T>G , CM000681.2:g.7128859T>G GRCh38
NC_000019.9:g.7128870T>G , CM000681.1:g.7128870T>G GRCh37
NC_000019.8:g.7079870T>G NCBI36
NG_008852.2:g.170142A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.2938A>C MANE Select ENSP00000303830.4:p.Arg980=
ENST00000302850.9:c.2938A>C ENSP00000303830.4:p.Arg980=
ENST00000341500.9:c.2902A>C ENSP00000342838.4:p.Arg968=
NM_000208.2:c.2938A>C NP_000199.2:p.Arg980=
NM_000208.3:c.2938A>C NP_000199.2:p.Arg980=
NM_001079817.1:c.2902A>C NP_001073285.1:p.Arg968=
NM_001079817.2:c.2902A>C NP_001073285.1:p.Arg968=
XM_011527988.1:c.3013A>C XP_011526290.1:p.Arg1005=
XM_011527989.1:c.2977A>C XP_011526291.1:p.Arg993=
XM_011527988.2:c.2935A>C XP_011526290.2:p.Arg979=
XM_011527989.3:c.2899A>C XP_011526291.2:p.Arg967=
NM_000208.4:c.2938A>C MANE Select NP_000199.2:p.Arg980=
NM_001079817.3:c.2902A>C NP_001073285.1:p.Arg968=