Canonical Allele Identifier: CA913190457

Gene: INSR

Linked Data

• ClinVar Variation Id: 594684
• ClinVar RCV Id: RCV000730034 ; RCV002507293
• dbSNP Id: rs1568470641

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184644_7184646delinsG , CM000681.2:g.7184644_7184646delinsG	GRCh38
NC_000019.9:g.7184655_7184657delinsG , CM000681.1:g.7184655_7184657delinsG	GRCh37
NC_000019.8:g.7135655_7135657delinsG	NCBI36
NG_008852.2:g.114355_114357delinsC

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.653-9_653-7delinsC MANE Select	ENSP00000303830.4:n.653-9_653-7delinsC
ENST00000302850.9:c.653-9_653-7delinsC	ENSP00000303830.4:n.653-9_653-7delinsC
ENST00000341500.9:c.653-9_653-7delinsC	ENSP00000342838.4:n.653-9_653-7delinsC
ENST00000598216.1:n.628-9_628-7delinsC
NM_000208.2:c.653-9_653-7delinsC	NP_000199.2:n.653-9_653-7delinsC
NM_000208.3:c.653-9_653-7delinsC	NP_000199.2:n.653-9_653-7delinsC
NM_001079817.1:c.653-9_653-7delinsC	NP_001073285.1:n.653-9_653-7delinsC
NM_001079817.2:c.653-9_653-7delinsC	NP_001073285.1:n.653-9_653-7delinsC
XM_011527988.1:c.731-9_731-7delinsC	XP_011526290.1:n.731-9_731-7delinsC
XM_011527989.1:c.731-9_731-7delinsC	XP_011526291.1:n.731-9_731-7delinsC
XM_011527988.2:c.653-9_653-7delinsC	XP_011526290.2:n.653-9_653-7delinsC
XM_011527989.3:c.653-9_653-7delinsC	XP_011526291.2:n.653-9_653-7delinsC
NM_000208.4:c.653-9_653-7delinsC MANE Select	NP_000199.2:n.653-9_653-7delinsC
NM_001079817.3:c.653-9_653-7delinsC	NP_001073285.1:n.653-9_653-7delinsC