Canonical Allele Identifier: CA304866813

Gene: INSR

Linked Data

• ClinVar Variation Id: 435513
• ClinVar RCV Id: RCV000501484
• dbSNP Id: rs1555746859
• MyVariant Identifiers: chr19:g.7184652_7184653insGA (hg19) ; chr19:g.7184641_7184642insGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184641_7184642insGA , CM000681.2:g.7184641_7184642insGA	GRCh38
NC_000019.9:g.7184652_7184653insGA , CM000681.1:g.7184652_7184653insGA	GRCh37
NC_000019.8:g.7135652_7135653insGA	NCBI36
NG_008852.2:g.114359_114360insTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.653-5_653-4insTC MANE Select	ENSP00000303830.4:n.653-5_653-4insTC
ENST00000302850.9:c.653-5_653-4insTC	ENSP00000303830.4:n.653-5_653-4insTC
ENST00000341500.9:c.653-5_653-4insTC	ENSP00000342838.4:n.653-5_653-4insTC
ENST00000598216.1:n.628-5_628-4insTC
NM_000208.2:c.653-5_653-4insTC	NP_000199.2:n.653-5_653-4insTC
NM_000208.3:c.653-5_653-4insTC	NP_000199.2:n.653-5_653-4insTC
NM_001079817.1:c.653-5_653-4insTC	NP_001073285.1:n.653-5_653-4insTC
NM_001079817.2:c.653-5_653-4insTC	NP_001073285.1:n.653-5_653-4insTC
XM_011527988.1:c.731-5_731-4insTC	XP_011526290.1:n.731-5_731-4insTC
XM_011527989.1:c.731-5_731-4insTC	XP_011526291.1:n.731-5_731-4insTC
XM_011527988.2:c.653-5_653-4insTC	XP_011526290.2:n.653-5_653-4insTC
XM_011527989.3:c.653-5_653-4insTC	XP_011526291.2:n.653-5_653-4insTC
NM_000208.4:c.653-5_653-4insTC MANE Select	NP_000199.2:n.653-5_653-4insTC
NM_001079817.3:c.653-5_653-4insTC	NP_001073285.1:n.653-5_653-4insTC