Canonical Allele Identifier: CA2320809775

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211678_7211679delinsGA , CM000681.2:g.7211678_7211679delinsGA	GRCh38
NC_000019.9:g.7211689_7211690delinsGA , CM000681.1:g.7211689_7211690delinsGA	GRCh37
NC_000019.8:g.7162689_7162690delinsGA	NCBI36
NG_008852.2:g.87322_87323delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27042_653-27041delinsTC MANE Select	ENSP00000303830.4:n.653-27042_653-27041delinsTC
ENST00000302850.9:c.653-27042_653-27041delinsTC	ENSP00000303830.4:n.653-27042_653-27041delinsTC
ENST00000341500.9:c.653-27042_653-27041delinsTC	ENSP00000342838.4:n.653-27042_653-27041delinsTC
ENST00000598216.1:n.628-27042_628-27041delinsTC
NM_000208.2:c.653-27042_653-27041delinsTC	NP_000199.2:n.653-27042_653-27041delinsTC
NM_000208.3:c.653-27042_653-27041delinsTC	NP_000199.2:n.653-27042_653-27041delinsTC
NM_001079817.1:c.653-27042_653-27041delinsTC	NP_001073285.1:n.653-27042_653-27041delinsTC
NM_001079817.2:c.653-27042_653-27041delinsTC	NP_001073285.1:n.653-27042_653-27041delinsTC
XM_011527988.1:c.731-27042_731-27041delinsTC	XP_011526290.1:n.731-27042_731-27041delinsTC
XM_011527989.1:c.731-27042_731-27041delinsTC	XP_011526291.1:n.731-27042_731-27041delinsTC
XM_011527988.2:c.653-27042_653-27041delinsTC	XP_011526290.2:n.653-27042_653-27041delinsTC
XM_011527989.3:c.653-27042_653-27041delinsTC	XP_011526291.2:n.653-27042_653-27041delinsTC
NM_000208.4:c.653-27042_653-27041delinsTC MANE Select	NP_000199.2:n.653-27042_653-27041delinsTC
NM_001079817.3:c.653-27042_653-27041delinsTC	NP_001073285.1:n.653-27042_653-27041delinsTC