Canonical Allele Identifier: CA993118079

Gene: INSR

Linked Data

• dbSNP Id: rs2034259335
• gnomAD v3: 19-7205064-A-ACTC
• gnomAD v4: 19-7205064-A-ACTC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7205065_7205066insTCC , CM000681.2:g.7205065_7205066insTCC	GRCh38
NC_000019.9:g.7205076_7205077insTCC , CM000681.1:g.7205076_7205077insTCC	GRCh37
NC_000019.8:g.7156076_7156077insTCC	NCBI36
NG_008852.2:g.93936_93937insGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-20428_653-20427insGAG MANE Select	ENSP00000303830.4:n.653-20428_653-20427insGAG
ENST00000302850.9:c.653-20428_653-20427insGAG	ENSP00000303830.4:n.653-20428_653-20427insGAG
ENST00000341500.9:c.653-20428_653-20427insGAG	ENSP00000342838.4:n.653-20428_653-20427insGAG
ENST00000598216.1:n.628-20428_628-20427insGAG
NM_000208.2:c.653-20428_653-20427insGAG	NP_000199.2:n.653-20428_653-20427insGAG
NM_000208.3:c.653-20428_653-20427insGAG	NP_000199.2:n.653-20428_653-20427insGAG
NM_001079817.1:c.653-20428_653-20427insGAG	NP_001073285.1:n.653-20428_653-20427insGAG
NM_001079817.2:c.653-20428_653-20427insGAG	NP_001073285.1:n.653-20428_653-20427insGAG
XM_011527988.1:c.731-20428_731-20427insGAG	XP_011526290.1:n.731-20428_731-20427insGAG
XM_011527989.1:c.731-20428_731-20427insGAG	XP_011526291.1:n.731-20428_731-20427insGAG
XM_011527988.2:c.653-20428_653-20427insGAG	XP_011526290.2:n.653-20428_653-20427insGAG
XM_011527989.3:c.653-20428_653-20427insGAG	XP_011526291.2:n.653-20428_653-20427insGAG
NM_000208.4:c.653-20428_653-20427insGAG MANE Select	NP_000199.2:n.653-20428_653-20427insGAG
NM_001079817.3:c.653-20428_653-20427insGAG	NP_001073285.1:n.653-20428_653-20427insGAG