Canonical Allele Identifier: CA2320788386

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166611_7166613delinsATC , CM000681.2:g.7166611_7166613delinsATC	GRCh38
NC_000019.9:g.7166622_7166624delinsATC , CM000681.1:g.7166622_7166624delinsATC	GRCh37
NC_000019.8:g.7117622_7117624delinsATC	NCBI36
NG_008852.2:g.132388_132390delinsGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1611-209_1611-207delinsGAT MANE Select	ENSP00000303830.4:n.1611-209_1611-207delinsGAT
ENST00000302850.9:c.1611-209_1611-207delinsGAT	ENSP00000303830.4:n.1611-209_1611-207delinsGAT
ENST00000341500.9:c.1611-209_1611-207delinsGAT	ENSP00000342838.4:n.1611-209_1611-207delinsGAT
ENST00000598216.1:n.1586-209_1586-207delinsGAT
ENST00000600492.1:c.12-209_12-207delinsGAT	ENSP00000473170.1:n.12-209_12-207delinsGAT
NM_000208.2:c.1611-209_1611-207delinsGAT	NP_000199.2:n.1611-209_1611-207delinsGAT
NM_000208.3:c.1611-209_1611-207delinsGAT	NP_000199.2:n.1611-209_1611-207delinsGAT
NM_001079817.1:c.1611-209_1611-207delinsGAT	NP_001073285.1:n.1611-209_1611-207delinsGAT
NM_001079817.2:c.1611-209_1611-207delinsGAT	NP_001073285.1:n.1611-209_1611-207delinsGAT
XM_011527988.1:c.1689-209_1689-207delinsGAT	XP_011526290.1:n.1689-209_1689-207delinsGAT
XM_011527989.1:c.1689-209_1689-207delinsGAT	XP_011526291.1:n.1689-209_1689-207delinsGAT
XM_011527988.2:c.1611-209_1611-207delinsGAT	XP_011526290.2:n.1611-209_1611-207delinsGAT
XM_011527989.3:c.1611-209_1611-207delinsGAT	XP_011526291.2:n.1611-209_1611-207delinsGAT
NM_000208.4:c.1611-209_1611-207delinsGAT MANE Select	NP_000199.2:n.1611-209_1611-207delinsGAT
NM_001079817.3:c.1611-209_1611-207delinsGAT	NP_001073285.1:n.1611-209_1611-207delinsGAT