Canonical Allele Identifier: CA884188298

Gene: INSR

Linked Data

• dbSNP Id: rs3835070
• gnomAD v3: 19-7184640-G-GGAGAGAGAGAGAGA
• gnomAD v4: 19-7184640-G-GGAGAGAGAGAGAGA
• MyVariant Identifiers: chr19:g.7184651_7184652insGAGAGAGAGAGAGA (hg19) ; chr19:g.7184640_7184641insGAGAGAGAGAGAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184648_7184661dup , CM000681.2:g.7184648_7184661dup	GRCh38
NC_000019.9:g.7184659_7184672dup , CM000681.1:g.7184659_7184672dup	GRCh37
NC_000019.8:g.7135659_7135672dup	NCBI36
NG_008852.2:g.114347_114360dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.653-17_653-4dup MANE Select	ENSP00000303830.4:n.653-17_653-4dup
ENST00000302850.9:c.653-17_653-4dup	ENSP00000303830.4:n.653-17_653-4dup
ENST00000341500.9:c.653-17_653-4dup	ENSP00000342838.4:n.653-17_653-4dup
ENST00000598216.1:n.628-17_628-4dup
NM_000208.2:c.653-17_653-4dup	NP_000199.2:n.653-17_653-4dup
NM_000208.3:c.653-17_653-4dup	NP_000199.2:n.653-17_653-4dup
NM_001079817.1:c.653-17_653-4dup	NP_001073285.1:n.653-17_653-4dup
NM_001079817.2:c.653-17_653-4dup	NP_001073285.1:n.653-17_653-4dup
XM_011527988.1:c.731-17_731-4dup	XP_011526290.1:n.731-17_731-4dup
XM_011527989.1:c.731-17_731-4dup	XP_011526291.1:n.731-17_731-4dup
XM_011527988.2:c.653-17_653-4dup	XP_011526290.2:n.653-17_653-4dup
XM_011527989.3:c.653-17_653-4dup	XP_011526291.2:n.653-17_653-4dup
NM_000208.4:c.653-17_653-4dup MANE Select	NP_000199.2:n.653-17_653-4dup
NM_001079817.3:c.653-17_653-4dup	NP_001073285.1:n.653-17_653-4dup