Canonical Allele Identifier: CA505400337
Gene: INSR HGNC NCBI

Linked Data

gnomAD v4: 19-7184387-G-A
MyVariant Identifiers: chr19:g.7184398G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7184387G>A , CM000681.2:g.7184387G>A GRCh38
NC_000019.9:g.7184398G>A , CM000681.1:g.7184398G>A GRCh37
NC_000019.8:g.7135398G>A NCBI36
NG_008852.2:g.114614C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.903C>T MANE Select ENSP00000303830.4:p.Cys301=
ENST00000302850.9:c.903C>T ENSP00000303830.4:p.Cys301=
ENST00000341500.9:c.903C>T ENSP00000342838.4:p.Cys301=
ENST00000598216.1:n.878C>T
NM_000208.2:c.903C>T NP_000199.2:p.Cys301=
NM_000208.3:c.903C>T NP_000199.2:p.Cys301=
NM_001079817.1:c.903C>T NP_001073285.1:p.Cys301=
NM_001079817.2:c.903C>T NP_001073285.1:p.Cys301=
XM_011527988.1:c.981C>T XP_011526290.1:p.Cys327=
XM_011527989.1:c.981C>T XP_011526291.1:p.Cys327=
XM_011527988.2:c.903C>T XP_011526290.2:p.Cys301=
XM_011527989.3:c.903C>T XP_011526291.2:p.Cys301=
NM_000208.4:c.903C>T MANE Select NP_000199.2:p.Cys301=
NM_001079817.3:c.903C>T NP_001073285.1:p.Cys301=