Canonical Allele Identifier: CA2545872211

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132189del , CM000681.2:g.7132189del	GRCh38
NC_000019.9:g.7132200del , CM000681.1:g.7132200del	GRCh37
NC_000019.8:g.7083200del	NCBI36
NG_008852.2:g.166813del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2812del MANE Select	ENSP00000303830.4:p.Glu938AsnfsTer7
ENST00000302850.9:c.2812del	ENSP00000303830.4:p.Glu938AsnfsTer7
ENST00000341500.9:c.2776del	ENSP00000342838.4:p.Glu926AsnfsTer7
NM_000208.2:c.2812del	NP_000199.2:p.Glu938AsnfsTer7
NM_000208.3:c.2812del	NP_000199.2:p.Glu938AsnfsTer7
NM_001079817.1:c.2776del	NP_001073285.1:p.Glu926AsnfsTer7
NM_001079817.2:c.2776del	NP_001073285.1:p.Glu926AsnfsTer7
XM_011527988.1:c.2890del	XP_011526290.1:p.Glu964AsnfsTer7
XM_011527989.1:c.2854del	XP_011526291.1:p.Glu952AsnfsTer7
XM_011527988.2:c.2812del	XP_011526290.2:p.Glu938AsnfsTer7
XM_011527989.3:c.2776del	XP_011526291.2:p.Glu926AsnfsTer7
NM_000208.4:c.2812del MANE Select	NP_000199.2:p.Glu938AsnfsTer7
NM_001079817.3:c.2776del	NP_001073285.1:p.Glu926AsnfsTer7