Canonical Allele Identifier: CA891862962

Gene: INSR

Linked Data

• ClinVar Variation Id: 592010
• ClinVar RCV Id: RCV000723193
• dbSNP Id: rs1568441899

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7142971_7142974dup , CM000681.2:g.7142971_7142974dup	GRCh38
NC_000019.9:g.7142982_7142985dup , CM000681.1:g.7142982_7142985dup	GRCh37
NC_000019.8:g.7093982_7093985dup	NCBI36
NG_008852.2:g.156027_156030dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2384_2387dup MANE Select	ENSP00000303830.4:p.Pro797GlnfsTer4
ENST00000302850.9:c.2384_2387dup	ENSP00000303830.4:p.Pro797GlnfsTer4
ENST00000341500.9:c.2348_2351dup	ENSP00000342838.4:p.Pro785GlnfsTer4
ENST00000597211.1:n.67_70dup
NM_000208.2:c.2384_2387dup	NP_000199.2:p.Pro797GlnfsTer4
NM_000208.3:c.2384_2387dup	NP_000199.2:p.Pro797GlnfsTer4
NM_001079817.1:c.2348_2351dup	NP_001073285.1:p.Pro785GlnfsTer4
NM_001079817.2:c.2348_2351dup	NP_001073285.1:p.Pro785GlnfsTer4
XM_011527988.1:c.2462_2465dup	XP_011526290.1:p.Pro823GlnfsTer4
XM_011527989.1:c.2426_2429dup	XP_011526291.1:p.Pro811GlnfsTer4
XM_011527988.2:c.2384_2387dup	XP_011526290.2:p.Pro797GlnfsTer4
XM_011527989.3:c.2348_2351dup	XP_011526291.2:p.Pro785GlnfsTer4
NM_000208.4:c.2384_2387dup MANE Select	NP_000199.2:p.Pro797GlnfsTer4
NM_001079817.3:c.2348_2351dup	NP_001073285.1:p.Pro785GlnfsTer4