Canonical Allele Identifier: CA304867030

Gene: INSR

Linked Data

• dbSNP Id: rs1555746893
• COSMIC: COSN23262458
• MyVariant Identifiers: chr19:g.7184675_7184676insAAAT (hg19) ; chr19:g.7184664_7184665insAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184666_7184667insATAA , CM000681.2:g.7184666_7184667insATAA	GRCh38
NC_000019.9:g.7184677_7184678insATAA , CM000681.1:g.7184677_7184678insATAA	GRCh37
NC_000019.8:g.7135677_7135678insATAA	NCBI36
NG_008852.2:g.114336_114337insATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-28_653-27insATTT MANE Select	ENSP00000303830.4:n.653-28_653-27insATTT
ENST00000302850.9:c.653-28_653-27insATTT	ENSP00000303830.4:n.653-28_653-27insATTT
ENST00000341500.9:c.653-28_653-27insATTT	ENSP00000342838.4:n.653-28_653-27insATTT
ENST00000598216.1:n.628-28_628-27insATTT
NM_000208.2:c.653-28_653-27insATTT	NP_000199.2:n.653-28_653-27insATTT
NM_000208.3:c.653-28_653-27insATTT	NP_000199.2:n.653-28_653-27insATTT
NM_001079817.1:c.653-28_653-27insATTT	NP_001073285.1:n.653-28_653-27insATTT
NM_001079817.2:c.653-28_653-27insATTT	NP_001073285.1:n.653-28_653-27insATTT
XM_011527988.1:c.731-28_731-27insATTT	XP_011526290.1:n.731-28_731-27insATTT
XM_011527989.1:c.731-28_731-27insATTT	XP_011526291.1:n.731-28_731-27insATTT
XM_011527988.2:c.653-28_653-27insATTT	XP_011526290.2:n.653-28_653-27insATTT
XM_011527989.3:c.653-28_653-27insATTT	XP_011526291.2:n.653-28_653-27insATTT
NM_000208.4:c.653-28_653-27insATTT MANE Select	NP_000199.2:n.653-28_653-27insATTT
NM_001079817.3:c.653-28_653-27insATTT	NP_001073285.1:n.653-28_653-27insATTT