Canonical Allele Identifier: CA993124924

Gene: INSR

Linked Data

• dbSNP Id: rs1555746897
• gnomAD v3: 19-7184666-A-AGAGAGAGAGG
• gnomAD v4: 19-7184666-A-AGAGAGAGAGG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184666_7184667insGAGAGAGAGG , CM000681.2:g.7184666_7184667insGAGAGAGAGG	GRCh38
NC_000019.9:g.7184677_7184678insGAGAGAGAGG , CM000681.1:g.7184677_7184678insGAGAGAGAGG	GRCh37
NC_000019.8:g.7135677_7135678insGAGAGAGAGG	NCBI36
NG_008852.2:g.114334_114335insCCTCTCTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-30_653-29insCCTCTCTCTC MANE Select	ENSP00000303830.4:n.653-30_653-29insCCTCTCTCTC
ENST00000302850.9:c.653-30_653-29insCCTCTCTCTC	ENSP00000303830.4:n.653-30_653-29insCCTCTCTCTC
ENST00000341500.9:c.653-30_653-29insCCTCTCTCTC	ENSP00000342838.4:n.653-30_653-29insCCTCTCTCTC
ENST00000598216.1:n.628-30_628-29insCCTCTCTCTC
NM_000208.2:c.653-30_653-29insCCTCTCTCTC	NP_000199.2:n.653-30_653-29insCCTCTCTCTC
NM_000208.3:c.653-30_653-29insCCTCTCTCTC	NP_000199.2:n.653-30_653-29insCCTCTCTCTC
NM_001079817.1:c.653-30_653-29insCCTCTCTCTC	NP_001073285.1:n.653-30_653-29insCCTCTCTCTC
NM_001079817.2:c.653-30_653-29insCCTCTCTCTC	NP_001073285.1:n.653-30_653-29insCCTCTCTCTC
XM_011527988.1:c.731-30_731-29insCCTCTCTCTC	XP_011526290.1:n.731-30_731-29insCCTCTCTCTC
XM_011527989.1:c.731-30_731-29insCCTCTCTCTC	XP_011526291.1:n.731-30_731-29insCCTCTCTCTC
XM_011527988.2:c.653-30_653-29insCCTCTCTCTC	XP_011526290.2:n.653-30_653-29insCCTCTCTCTC
XM_011527989.3:c.653-30_653-29insCCTCTCTCTC	XP_011526291.2:n.653-30_653-29insCCTCTCTCTC
NM_000208.4:c.653-30_653-29insCCTCTCTCTC MANE Select	NP_000199.2:n.653-30_653-29insCCTCTCTCTC
NM_001079817.3:c.653-30_653-29insCCTCTCTCTC	NP_001073285.1:n.653-30_653-29insCCTCTCTCTC