Canonical Allele Identifier: CA631723723

Gene: INSR

Linked Data

• dbSNP Id: rs1555746888
• gnomAD v2: 19-7184674-G-GGAAAT
• gnomAD v3: 19-7184663-G-GGAAAT
• gnomAD v4: 19-7184663-G-GGAAAT
• MyVariant Identifiers: chr19:g.7184675_7184686delinsGAAATAAATAAATAAAT (hg19) ; chr19:g.7184664_7184675delinsGAAATAAATAAATAAAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184663_7184664insGAAAT , CM000681.2:g.7184663_7184664insGAAAT	GRCh38
NC_000019.9:g.7184674_7184675insGAAAT , CM000681.1:g.7184674_7184675insGAAAT	GRCh37
NC_000019.8:g.7135674_7135675insGAAAT	NCBI36
NG_008852.2:g.114337_114338insATTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27_653-26insATTTC MANE Select	ENSP00000303830.4:n.653-27_653-26insATTTC
ENST00000302850.9:c.653-27_653-26insATTTC	ENSP00000303830.4:n.653-27_653-26insATTTC
ENST00000341500.9:c.653-27_653-26insATTTC	ENSP00000342838.4:n.653-27_653-26insATTTC
ENST00000598216.1:n.628-27_628-26insATTTC
NM_000208.2:c.653-27_653-26insATTTC	NP_000199.2:n.653-27_653-26insATTTC
NM_000208.3:c.653-27_653-26insATTTC	NP_000199.2:n.653-27_653-26insATTTC
NM_001079817.1:c.653-27_653-26insATTTC	NP_001073285.1:n.653-27_653-26insATTTC
NM_001079817.2:c.653-27_653-26insATTTC	NP_001073285.1:n.653-27_653-26insATTTC
XM_011527988.1:c.731-27_731-26insATTTC	XP_011526290.1:n.731-27_731-26insATTTC
XM_011527989.1:c.731-27_731-26insATTTC	XP_011526291.1:n.731-27_731-26insATTTC
XM_011527988.2:c.653-27_653-26insATTTC	XP_011526290.2:n.653-27_653-26insATTTC
XM_011527989.3:c.653-27_653-26insATTTC	XP_011526291.2:n.653-27_653-26insATTTC
NM_000208.4:c.653-27_653-26insATTTC MANE Select	NP_000199.2:n.653-27_653-26insATTTC
NM_001079817.3:c.653-27_653-26insATTTC	NP_001073285.1:n.653-27_653-26insATTTC