Canonical Allele Identifier: CA631693447

Gene: INSR

Linked Data

• dbSNP Id: rs1163718658
• gnomAD v2: 19-7184705-A-ATAAG
• gnomAD v3: 19-7184694-A-ATAAG
• gnomAD v4: 19-7184694-A-ATAAG
• MyVariant Identifiers: chr19:g.7184705_7184706insTAAG (hg19) ; chr19:g.7184694_7184695insTAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184697_7184698insGTAA , CM000681.2:g.7184697_7184698insGTAA	GRCh38
NC_000019.9:g.7184708_7184709insGTAA , CM000681.1:g.7184708_7184709insGTAA	GRCh37
NC_000019.8:g.7135708_7135709insGTAA	NCBI36
NG_008852.2:g.114306_114307insCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-58_653-57insCTTA MANE Select	ENSP00000303830.4:n.653-58_653-57insCTTA
ENST00000302850.9:c.653-58_653-57insCTTA	ENSP00000303830.4:n.653-58_653-57insCTTA
ENST00000341500.9:c.653-58_653-57insCTTA	ENSP00000342838.4:n.653-58_653-57insCTTA
ENST00000598216.1:n.628-58_628-57insCTTA
NM_000208.2:c.653-58_653-57insCTTA	NP_000199.2:n.653-58_653-57insCTTA
NM_000208.3:c.653-58_653-57insCTTA	NP_000199.2:n.653-58_653-57insCTTA
NM_001079817.1:c.653-58_653-57insCTTA	NP_001073285.1:n.653-58_653-57insCTTA
NM_001079817.2:c.653-58_653-57insCTTA	NP_001073285.1:n.653-58_653-57insCTTA
XM_011527988.1:c.731-58_731-57insCTTA	XP_011526290.1:n.731-58_731-57insCTTA
XM_011527989.1:c.731-58_731-57insCTTA	XP_011526291.1:n.731-58_731-57insCTTA
XM_011527988.2:c.653-58_653-57insCTTA	XP_011526290.2:n.653-58_653-57insCTTA
XM_011527989.3:c.653-58_653-57insCTTA	XP_011526291.2:n.653-58_653-57insCTTA
NM_000208.4:c.653-58_653-57insCTTA MANE Select	NP_000199.2:n.653-58_653-57insCTTA
NM_001079817.3:c.653-58_653-57insCTTA	NP_001073285.1:n.653-58_653-57insCTTA