Canonical Allele Identifier: CA9136051

Gene: INSR

Linked Data

• dbSNP Id: rs762439383
• ExAC: 19:7184668 G / GAGAC
• gnomAD v2: 19-7184668-G-GAGAC
• gnomAD v3: 19-7184657-G-GAGAC
• gnomAD v4: 19-7184657-G-GAGAC
• MyVariant Identifiers: chr19:g.7184671_7184672insCAGA (hg19) ; chr19:g.7184668_7184669insAGAC (hg19) ; chr19:g.7184660_7184661insCAGA (hg38) ; chr19:g.7184657_7184658insAGAC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184660_7184661insCAGA , CM000681.2:g.7184660_7184661insCAGA	GRCh38
NC_000019.9:g.7184671_7184672insCAGA , CM000681.1:g.7184671_7184672insCAGA	GRCh37
NC_000019.8:g.7135671_7135672insCAGA	NCBI36
NG_008852.2:g.114343_114344insGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-21_653-20insGTCT MANE Select	ENSP00000303830.4:n.653-21_653-20insGTCT
ENST00000302850.9:c.653-21_653-20insGTCT	ENSP00000303830.4:n.653-21_653-20insGTCT
ENST00000341500.9:c.653-21_653-20insGTCT	ENSP00000342838.4:n.653-21_653-20insGTCT
ENST00000598216.1:n.628-21_628-20insGTCT
NM_000208.2:c.653-21_653-20insGTCT	NP_000199.2:n.653-21_653-20insGTCT
NM_000208.3:c.653-21_653-20insGTCT	NP_000199.2:n.653-21_653-20insGTCT
NM_001079817.1:c.653-21_653-20insGTCT	NP_001073285.1:n.653-21_653-20insGTCT
NM_001079817.2:c.653-21_653-20insGTCT	NP_001073285.1:n.653-21_653-20insGTCT
XM_011527988.1:c.731-21_731-20insGTCT	XP_011526290.1:n.731-21_731-20insGTCT
XM_011527989.1:c.731-21_731-20insGTCT	XP_011526291.1:n.731-21_731-20insGTCT
XM_011527988.2:c.653-21_653-20insGTCT	XP_011526290.2:n.653-21_653-20insGTCT
XM_011527989.3:c.653-21_653-20insGTCT	XP_011526291.2:n.653-21_653-20insGTCT
NM_000208.4:c.653-21_653-20insGTCT MANE Select	NP_000199.2:n.653-21_653-20insGTCT
NM_001079817.3:c.653-21_653-20insGTCT	NP_001073285.1:n.653-21_653-20insGTCT