Canonical Allele Identifier: CA2320796183

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184696_7184703delinsAAATAAAT , CM000681.2:g.7184696_7184703delinsAAATAAAT	GRCh38
NC_000019.9:g.7184707_7184714delinsAAATAAAT , CM000681.1:g.7184707_7184714delinsAAATAAAT	GRCh37
NC_000019.8:g.7135707_7135714delinsAAATAAAT	NCBI36
NG_008852.2:g.114298_114305delinsATTTATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-66_653-59delinsATTTATTT MANE Select	ENSP00000303830.4:n.653-66_653-59delinsATTTATTT
ENST00000302850.9:c.653-66_653-59delinsATTTATTT	ENSP00000303830.4:n.653-66_653-59delinsATTTATTT
ENST00000341500.9:c.653-66_653-59delinsATTTATTT	ENSP00000342838.4:n.653-66_653-59delinsATTTATTT
ENST00000598216.1:n.628-66_628-59delinsATTTATTT
NM_000208.2:c.653-66_653-59delinsATTTATTT	NP_000199.2:n.653-66_653-59delinsATTTATTT
NM_000208.3:c.653-66_653-59delinsATTTATTT	NP_000199.2:n.653-66_653-59delinsATTTATTT
NM_001079817.1:c.653-66_653-59delinsATTTATTT	NP_001073285.1:n.653-66_653-59delinsATTTATTT
NM_001079817.2:c.653-66_653-59delinsATTTATTT	NP_001073285.1:n.653-66_653-59delinsATTTATTT
XM_011527988.1:c.731-66_731-59delinsATTTATTT	XP_011526290.1:n.731-66_731-59delinsATTTATTT
XM_011527989.1:c.731-66_731-59delinsATTTATTT	XP_011526291.1:n.731-66_731-59delinsATTTATTT
XM_011527988.2:c.653-66_653-59delinsATTTATTT	XP_011526290.2:n.653-66_653-59delinsATTTATTT
XM_011527989.3:c.653-66_653-59delinsATTTATTT	XP_011526291.2:n.653-66_653-59delinsATTTATTT
NM_000208.4:c.653-66_653-59delinsATTTATTT MANE Select	NP_000199.2:n.653-66_653-59delinsATTTATTT
NM_001079817.3:c.653-66_653-59delinsATTTATTT	NP_001073285.1:n.653-66_653-59delinsATTTATTT