Canonical Allele Identifier: CA2587926404

Gene: INSR

Linked Data

• gnomAD v4: 19-7184673-A-AATAG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184676_7184677insGATA , CM000681.2:g.7184676_7184677insGATA	GRCh38
NC_000019.9:g.7184687_7184688insGATA , CM000681.1:g.7184687_7184688insGATA	GRCh37
NC_000019.8:g.7135687_7135688insGATA	NCBI36
NG_008852.2:g.114327_114328insCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-37_653-36insCTAT MANE Select	ENSP00000303830.4:n.653-37_653-36insCTAT
ENST00000302850.9:c.653-37_653-36insCTAT	ENSP00000303830.4:n.653-37_653-36insCTAT
ENST00000341500.9:c.653-37_653-36insCTAT	ENSP00000342838.4:n.653-37_653-36insCTAT
ENST00000598216.1:n.628-37_628-36insCTAT
NM_000208.2:c.653-37_653-36insCTAT	NP_000199.2:n.653-37_653-36insCTAT
NM_000208.3:c.653-37_653-36insCTAT	NP_000199.2:n.653-37_653-36insCTAT
NM_001079817.1:c.653-37_653-36insCTAT	NP_001073285.1:n.653-37_653-36insCTAT
NM_001079817.2:c.653-37_653-36insCTAT	NP_001073285.1:n.653-37_653-36insCTAT
XM_011527988.1:c.731-37_731-36insCTAT	XP_011526290.1:n.731-37_731-36insCTAT
XM_011527989.1:c.731-37_731-36insCTAT	XP_011526291.1:n.731-37_731-36insCTAT
XM_011527988.2:c.653-37_653-36insCTAT	XP_011526290.2:n.653-37_653-36insCTAT
XM_011527989.3:c.653-37_653-36insCTAT	XP_011526291.2:n.653-37_653-36insCTAT
NM_000208.4:c.653-37_653-36insCTAT MANE Select	NP_000199.2:n.653-37_653-36insCTAT
NM_001079817.3:c.653-37_653-36insCTAT	NP_001073285.1:n.653-37_653-36insCTAT