Canonical Allele Identifier: CA2695228090

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132220_7132221delinsT , CM000681.2:g.7132220_7132221delinsT	GRCh38
NC_000019.9:g.7132231_7132232delinsT , CM000681.1:g.7132231_7132232delinsT	GRCh37
NC_000019.8:g.7083231_7083232delinsT	NCBI36
NG_008852.2:g.166780_166781delinsA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2779_2780delinsA MANE Select	ENSP00000303830.4:p.Ala927ThrfsTer18
ENST00000302850.9:c.2779_2780delinsA	ENSP00000303830.4:p.Ala927ThrfsTer18
ENST00000341500.9:c.2743_2744delinsA	ENSP00000342838.4:p.Ala915ThrfsTer18
NM_000208.2:c.2779_2780delinsA	NP_000199.2:p.Ala927ThrfsTer18
NM_000208.3:c.2779_2780delinsA	NP_000199.2:p.Ala927ThrfsTer18
NM_001079817.1:c.2743_2744delinsA	NP_001073285.1:p.Ala915ThrfsTer18
NM_001079817.2:c.2743_2744delinsA	NP_001073285.1:p.Ala915ThrfsTer18
XM_011527988.1:c.2857_2858delinsA	XP_011526290.1:p.Ala953ThrfsTer18
XM_011527989.1:c.2821_2822delinsA	XP_011526291.1:p.Ala941ThrfsTer18
XM_011527988.2:c.2779_2780delinsA	XP_011526290.2:p.Ala927ThrfsTer18
XM_011527989.3:c.2743_2744delinsA	XP_011526291.2:p.Ala915ThrfsTer18
NM_000208.4:c.2779_2780delinsA MANE Select	NP_000199.2:p.Ala927ThrfsTer18
NM_001079817.3:c.2743_2744delinsA	NP_001073285.1:p.Ala915ThrfsTer18