Canonical Allele Identifier: CA2320769498

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128972_7128974delinsAAT , CM000681.2:g.7128972_7128974delinsAAT	GRCh38
NC_000019.9:g.7128983_7128985delinsAAT , CM000681.1:g.7128983_7128985delinsAAT	GRCh37
NC_000019.8:g.7079983_7079985delinsAAT	NCBI36
NG_008852.2:g.170027_170029delinsATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2843-20_2843-18delinsATT MANE Select	ENSP00000303830.4:n.2843-20_2843-18delins...
ENST00000302850.9:c.2843-20_2843-18delinsATT	ENSP00000303830.4:n.2843-20_2843-18delins...
ENST00000341500.9:c.2807-20_2807-18delinsATT	ENSP00000342838.4:n.2807-20_2807-18delins...
NM_000208.2:c.2843-20_2843-18delinsATT	NP_000199.2:n.2843-20_2843-18delinsATT
NM_000208.3:c.2843-20_2843-18delinsATT	NP_000199.2:n.2843-20_2843-18delinsATT
NM_001079817.1:c.2807-20_2807-18delinsATT	NP_001073285.1:n.2807-20_2807-18delinsATT...
NM_001079817.2:c.2807-20_2807-18delinsATT	NP_001073285.1:n.2807-20_2807-18delinsATT...
XM_011527988.1:c.2921-23_2921-21delinsATT	XP_011526290.1:n.2921-23_2921-21delinsATT...
XM_011527989.1:c.2885-23_2885-21delinsATT	XP_011526291.1:n.2885-23_2885-21delinsATT...
XM_011527988.2:c.2843-23_2843-21delinsATT	XP_011526290.2:n.2843-23_2843-21delinsATT...
XM_011527989.3:c.2807-23_2807-21delinsATT	XP_011526291.2:n.2807-23_2807-21delinsATT...
NM_000208.4:c.2843-20_2843-18delinsATT MANE Select	NP_000199.2:n.2843-20_2843-18delinsATT
NM_001079817.3:c.2807-20_2807-18delinsATT	NP_001073285.1:n.2807-20_2807-18delinsATT...