Canonical Allele Identifier: CA2320809930

Gene: INSR

Linked Data

• dbSNP Id: rs1875253832

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211926_7211933del , CM000681.2:g.7211926_7211933del	GRCh38
NC_000019.9:g.7211937_7211944del , CM000681.1:g.7211937_7211944del	GRCh37
NC_000019.8:g.7162937_7162944del	NCBI36
NG_008852.2:g.87068_87075del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27296_653-27289del MANE Select	ENSP00000303830.4:n.653-27296_653-27289del
ENST00000302850.9:c.653-27296_653-27289del	ENSP00000303830.4:n.653-27296_653-27289del
ENST00000341500.9:c.653-27296_653-27289del	ENSP00000342838.4:n.653-27296_653-27289del
ENST00000598216.1:n.628-27296_628-27289del
NM_000208.2:c.653-27296_653-27289del	NP_000199.2:n.653-27296_653-27289del
NM_000208.3:c.653-27296_653-27289del	NP_000199.2:n.653-27296_653-27289del
NM_001079817.1:c.653-27296_653-27289del	NP_001073285.1:n.653-27296_653-27289del
NM_001079817.2:c.653-27296_653-27289del	NP_001073285.1:n.653-27296_653-27289del
XM_011527988.1:c.731-27296_731-27289del	XP_011526290.1:n.731-27296_731-27289del
XM_011527989.1:c.731-27296_731-27289del	XP_011526291.1:n.731-27296_731-27289del
XM_011527988.2:c.653-27296_653-27289del	XP_011526290.2:n.653-27296_653-27289del
XM_011527989.3:c.653-27296_653-27289del	XP_011526291.2:n.653-27296_653-27289del
NM_000208.4:c.653-27296_653-27289del MANE Select	NP_000199.2:n.653-27296_653-27289del
NM_001079817.3:c.653-27296_653-27289del	NP_001073285.1:n.653-27296_653-27289del