Canonical Allele Identifier: CA2735510907

Gene: INSR

Linked Data

• dbSNP Id: rs2145074021

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211560_7211561del , CM000681.2:g.7211560_7211561del	GRCh38
NC_000019.9:g.7211571_7211572del , CM000681.1:g.7211571_7211572del	GRCh37
NC_000019.8:g.7162571_7162572del	NCBI36
NG_008852.2:g.87441_87442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-26923_653-26922del MANE Select	ENSP00000303830.4:n.653-26923_653-26922del
ENST00000302850.9:c.653-26923_653-26922del	ENSP00000303830.4:n.653-26923_653-26922del
ENST00000341500.9:c.653-26923_653-26922del	ENSP00000342838.4:n.653-26923_653-26922del
ENST00000598216.1:n.628-26923_628-26922del
NM_000208.2:c.653-26923_653-26922del	NP_000199.2:n.653-26923_653-26922del
NM_000208.3:c.653-26923_653-26922del	NP_000199.2:n.653-26923_653-26922del
NM_001079817.1:c.653-26923_653-26922del	NP_001073285.1:n.653-26923_653-26922del
NM_001079817.2:c.653-26923_653-26922del	NP_001073285.1:n.653-26923_653-26922del
XM_011527988.1:c.731-26923_731-26922del	XP_011526290.1:n.731-26923_731-26922del
XM_011527989.1:c.731-26923_731-26922del	XP_011526291.1:n.731-26923_731-26922del
XM_011527988.2:c.653-26923_653-26922del	XP_011526290.2:n.653-26923_653-26922del
XM_011527989.3:c.653-26923_653-26922del	XP_011526291.2:n.653-26923_653-26922del
NM_000208.4:c.653-26923_653-26922del MANE Select	NP_000199.2:n.653-26923_653-26922del
NM_001079817.3:c.653-26923_653-26922del	NP_001073285.1:n.653-26923_653-26922del