Canonical Allele Identifier: CA505400277
Gene: INSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr19:g.7125483G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7125472G>T , CM000681.2:g.7125472G>T GRCh38
NC_000019.9:g.7125483G>T , CM000681.1:g.7125483G>T GRCh37
NC_000019.8:g.7076483G>T NCBI36
NG_008852.2:g.173529C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.3069C>A MANE Select ENSP00000303830.4:p.Ile1023=
ENST00000302850.9:c.3069C>A ENSP00000303830.4:p.Ile1023=
ENST00000341500.9:c.3033C>A ENSP00000342838.4:p.Ile1011=
NM_000208.2:c.3069C>A NP_000199.2:p.Ile1023=
NM_000208.3:c.3069C>A NP_000199.2:p.Ile1023=
NM_001079817.1:c.3033C>A NP_001073285.1:p.Ile1011=
NM_001079817.2:c.3033C>A NP_001073285.1:p.Ile1011=
XM_011527988.1:c.3144C>A XP_011526290.1:p.Ile1048=
XM_011527989.1:c.3108C>A XP_011526291.1:p.Ile1036=
XM_011527988.2:c.3066C>A XP_011526290.2:p.Ile1022=
XM_011527989.3:c.3030C>A XP_011526291.2:p.Ile1010=
NM_000208.4:c.3069C>A MANE Select NP_000199.2:p.Ile1023=
NM_001079817.3:c.3033C>A NP_001073285.1:p.Ile1011=