Canonical Allele Identifier: CA2558584396

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211793_7211794insGAT , CM000681.2:g.7211793_7211794insGAT	GRCh38
NC_000019.9:g.7211804_7211805insGAT , CM000681.1:g.7211804_7211805insGAT	GRCh37
NC_000019.8:g.7162804_7162805insGAT	NCBI36
NG_008852.2:g.87207_87208insATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27157_653-27156insATC MANE Select	ENSP00000303830.4:n.653-27157_653-27156insATC
ENST00000302850.9:c.653-27157_653-27156insATC	ENSP00000303830.4:n.653-27157_653-27156insATC
ENST00000341500.9:c.653-27157_653-27156insATC	ENSP00000342838.4:n.653-27157_653-27156insATC
ENST00000598216.1:n.628-27157_628-27156insATC
NM_000208.2:c.653-27157_653-27156insATC	NP_000199.2:n.653-27157_653-27156insATC
NM_000208.3:c.653-27157_653-27156insATC	NP_000199.2:n.653-27157_653-27156insATC
NM_001079817.1:c.653-27157_653-27156insATC	NP_001073285.1:n.653-27157_653-27156insATC
NM_001079817.2:c.653-27157_653-27156insATC	NP_001073285.1:n.653-27157_653-27156insATC
XM_011527988.1:c.731-27157_731-27156insATC	XP_011526290.1:n.731-27157_731-27156insATC
XM_011527989.1:c.731-27157_731-27156insATC	XP_011526291.1:n.731-27157_731-27156insATC
XM_011527988.2:c.653-27157_653-27156insATC	XP_011526290.2:n.653-27157_653-27156insATC
XM_011527989.3:c.653-27157_653-27156insATC	XP_011526291.2:n.653-27157_653-27156insATC
NM_000208.4:c.653-27157_653-27156insATC MANE Select	NP_000199.2:n.653-27157_653-27156insATC
NM_001079817.3:c.653-27157_653-27156insATC	NP_001073285.1:n.653-27157_653-27156insATC