Canonical Allele Identifier: CA2320795991

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184643_7184644delinsGA , CM000681.2:g.7184643_7184644delinsGA	GRCh38
NC_000019.9:g.7184654_7184655delinsGA , CM000681.1:g.7184654_7184655delinsGA	GRCh37
NC_000019.8:g.7135654_7135655delinsGA	NCBI36
NG_008852.2:g.114357_114358delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.653-7_653-6delinsTC MANE Select	ENSP00000303830.4:n.653-7_653-6delinsTC
ENST00000302850.9:c.653-7_653-6delinsTC	ENSP00000303830.4:n.653-7_653-6delinsTC
ENST00000341500.9:c.653-7_653-6delinsTC	ENSP00000342838.4:n.653-7_653-6delinsTC
ENST00000598216.1:n.628-7_628-6delinsTC
NM_000208.2:c.653-7_653-6delinsTC	NP_000199.2:n.653-7_653-6delinsTC
NM_000208.3:c.653-7_653-6delinsTC	NP_000199.2:n.653-7_653-6delinsTC
NM_001079817.1:c.653-7_653-6delinsTC	NP_001073285.1:n.653-7_653-6delinsTC
NM_001079817.2:c.653-7_653-6delinsTC	NP_001073285.1:n.653-7_653-6delinsTC
XM_011527988.1:c.731-7_731-6delinsTC	XP_011526290.1:n.731-7_731-6delinsTC
XM_011527989.1:c.731-7_731-6delinsTC	XP_011526291.1:n.731-7_731-6delinsTC
XM_011527988.2:c.653-7_653-6delinsTC	XP_011526290.2:n.653-7_653-6delinsTC
XM_011527989.3:c.653-7_653-6delinsTC	XP_011526291.2:n.653-7_653-6delinsTC
NM_000208.4:c.653-7_653-6delinsTC MANE Select	NP_000199.2:n.653-7_653-6delinsTC
NM_001079817.3:c.653-7_653-6delinsTC	NP_001073285.1:n.653-7_653-6delinsTC