Canonical Allele Identifier: CA631723732

Gene: INSR

Linked Data

• dbSNP Id: rs1568470808
• gnomAD v2: 19-7184685-A-AGAGG
• gnomAD v3: 19-7184674-A-AGAGG
• gnomAD v4: 19-7184674-A-AGAGG
• MyVariant Identifiers: chr19:g.7184685_7184686insGAGG (hg19) ; chr19:g.7184674_7184675insGAGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184674_7184675insGAGG , CM000681.2:g.7184674_7184675insGAGG	GRCh38
NC_000019.9:g.7184685_7184686insGAGG , CM000681.1:g.7184685_7184686insGAGG	GRCh37
NC_000019.8:g.7135685_7135686insGAGG	NCBI36
NG_008852.2:g.114326_114327insCCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-38_653-37insCCTC MANE Select	ENSP00000303830.4:n.653-38_653-37insCCTC
ENST00000302850.9:c.653-38_653-37insCCTC	ENSP00000303830.4:n.653-38_653-37insCCTC
ENST00000341500.9:c.653-38_653-37insCCTC	ENSP00000342838.4:n.653-38_653-37insCCTC
ENST00000598216.1:n.628-38_628-37insCCTC
NM_000208.2:c.653-38_653-37insCCTC	NP_000199.2:n.653-38_653-37insCCTC
NM_000208.3:c.653-38_653-37insCCTC	NP_000199.2:n.653-38_653-37insCCTC
NM_001079817.1:c.653-38_653-37insCCTC	NP_001073285.1:n.653-38_653-37insCCTC
NM_001079817.2:c.653-38_653-37insCCTC	NP_001073285.1:n.653-38_653-37insCCTC
XM_011527988.1:c.731-38_731-37insCCTC	XP_011526290.1:n.731-38_731-37insCCTC
XM_011527989.1:c.731-38_731-37insCCTC	XP_011526291.1:n.731-38_731-37insCCTC
XM_011527988.2:c.653-38_653-37insCCTC	XP_011526290.2:n.653-38_653-37insCCTC
XM_011527989.3:c.653-38_653-37insCCTC	XP_011526291.2:n.653-38_653-37insCCTC
NM_000208.4:c.653-38_653-37insCCTC MANE Select	NP_000199.2:n.653-38_653-37insCCTC
NM_001079817.3:c.653-38_653-37insCCTC	NP_001073285.1:n.653-38_653-37insCCTC