Canonical Allele Identifier: CA505217502
Gene: INSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7132224G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7132213G>T , CM000681.2:g.7132213G>T GRCh38
NC_000019.9:g.7132224G>T , CM000681.1:g.7132224G>T GRCh37
NC_000019.8:g.7083224G>T NCBI36
NG_008852.2:g.166788C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.2787C>A MANE Select ENSP00000303830.4:p.Ser929=
ENST00000302850.9:c.2787C>A ENSP00000303830.4:p.Ser929=
ENST00000341500.9:c.2751C>A ENSP00000342838.4:p.Ser917=
NM_000208.2:c.2787C>A NP_000199.2:p.Ser929=
NM_000208.3:c.2787C>A NP_000199.2:p.Ser929=
NM_001079817.1:c.2751C>A NP_001073285.1:p.Ser917=
NM_001079817.2:c.2751C>A NP_001073285.1:p.Ser917=
XM_011527988.1:c.2865C>A XP_011526290.1:p.Ser955=
XM_011527989.1:c.2829C>A XP_011526291.1:p.Ser943=
XM_011527988.2:c.2787C>A XP_011526290.2:p.Ser929=
XM_011527989.3:c.2751C>A XP_011526291.2:p.Ser917=
NM_000208.4:c.2787C>A MANE Select NP_000199.2:p.Ser929=
NM_001079817.3:c.2751C>A NP_001073285.1:p.Ser917=