Canonical Allele Identifier: CA2813464194

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184651_7184652insGAGA , CM000681.2:g.7184651_7184652insGAGA	GRCh38
NC_000019.9:g.7184662_7184663insGAGA , CM000681.1:g.7184662_7184663insGAGA	GRCh37
NC_000019.8:g.7135662_7135663insGAGA	NCBI36
NG_008852.2:g.114349_114350insTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-15_653-14insTCTC MANE Select	ENSP00000303830.4:n.653-15_653-14insTCTC
ENST00000302850.9:c.653-15_653-14insTCTC	ENSP00000303830.4:n.653-15_653-14insTCTC
ENST00000341500.9:c.653-15_653-14insTCTC	ENSP00000342838.4:n.653-15_653-14insTCTC
ENST00000598216.1:n.628-15_628-14insTCTC
NM_000208.2:c.653-15_653-14insTCTC	NP_000199.2:n.653-15_653-14insTCTC
NM_000208.3:c.653-15_653-14insTCTC	NP_000199.2:n.653-15_653-14insTCTC
NM_001079817.1:c.653-15_653-14insTCTC	NP_001073285.1:n.653-15_653-14insTCTC
NM_001079817.2:c.653-15_653-14insTCTC	NP_001073285.1:n.653-15_653-14insTCTC
XM_011527988.1:c.731-15_731-14insTCTC	XP_011526290.1:n.731-15_731-14insTCTC
XM_011527989.1:c.731-15_731-14insTCTC	XP_011526291.1:n.731-15_731-14insTCTC
XM_011527988.2:c.653-15_653-14insTCTC	XP_011526290.2:n.653-15_653-14insTCTC
XM_011527989.3:c.653-15_653-14insTCTC	XP_011526291.2:n.653-15_653-14insTCTC
NM_000208.4:c.653-15_653-14insTCTC MANE Select	NP_000199.2:n.653-15_653-14insTCTC
NM_001079817.3:c.653-15_653-14insTCTC	NP_001073285.1:n.653-15_653-14insTCTC