Canonical Allele Identifier: CA9136055

Gene: INSR

Linked Data

• dbSNP Id: rs199750451
• ExAC: 19:7184672 G / GAGAGAGAGAGA
• gnomAD v2: 19-7184672-G-GAGAGAGAGAGA
• gnomAD v3: 19-7184661-G-GAGAGAGAGAGA
• gnomAD v4: 19-7184661-G-GAGAGAGAGAGA
• MyVariant Identifiers: chr19:g.7184672_7184673insAGAGAGAGAGA (hg19) ; chr19:g.7184661_7184662insAGAGAGAGAGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184661_7184662insAGAGAGAGAGA , CM000681.2:g.7184661_7184662insAGAGAGAGAGA	GRCh38
NC_000019.9:g.7184672_7184673insAGAGAGAGAGA , CM000681.1:g.7184672_7184673insAGAGAGAGAGA	GRCh37
NC_000019.8:g.7135672_7135673insAGAGAGAGAGA	NCBI36
NG_008852.2:g.114339_114340insTCTCTCTCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-25_653-24insTCTCTCTCTCT MANE Select	ENSP00000303830.4:n.653-25_653-24insTCTCTCTCTCT
ENST00000302850.9:c.653-25_653-24insTCTCTCTCTCT	ENSP00000303830.4:n.653-25_653-24insTCTCTCTCTCT
ENST00000341500.9:c.653-25_653-24insTCTCTCTCTCT	ENSP00000342838.4:n.653-25_653-24insTCTCTCTCTCT
ENST00000598216.1:n.628-25_628-24insTCTCTCTCTCT
NM_000208.2:c.653-25_653-24insTCTCTCTCTCT	NP_000199.2:n.653-25_653-24insTCTCTCTCTCT
NM_000208.3:c.653-25_653-24insTCTCTCTCTCT	NP_000199.2:n.653-25_653-24insTCTCTCTCTCT
NM_001079817.1:c.653-25_653-24insTCTCTCTCTCT	NP_001073285.1:n.653-25_653-24insTCTCTCTCTCT
NM_001079817.2:c.653-25_653-24insTCTCTCTCTCT	NP_001073285.1:n.653-25_653-24insTCTCTCTCTCT
XM_011527988.1:c.731-25_731-24insTCTCTCTCTCT	XP_011526290.1:n.731-25_731-24insTCTCTCTCTCT
XM_011527989.1:c.731-25_731-24insTCTCTCTCTCT	XP_011526291.1:n.731-25_731-24insTCTCTCTCTCT
XM_011527988.2:c.653-25_653-24insTCTCTCTCTCT	XP_011526290.2:n.653-25_653-24insTCTCTCTCTCT
XM_011527989.3:c.653-25_653-24insTCTCTCTCTCT	XP_011526291.2:n.653-25_653-24insTCTCTCTCTCT
NM_000208.4:c.653-25_653-24insTCTCTCTCTCT MANE Select	NP_000199.2:n.653-25_653-24insTCTCTCTCTCT
NM_001079817.3:c.653-25_653-24insTCTCTCTCTCT	NP_001073285.1:n.653-25_653-24insTCTCTCTCTCT