Canonical Allele Identifier: CA2320809796

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211715_7211716delinsGC , CM000681.2:g.7211715_7211716delinsGC	GRCh38
NC_000019.9:g.7211726_7211727delinsGC , CM000681.1:g.7211726_7211727delinsGC	GRCh37
NC_000019.8:g.7162726_7162727delinsGC	NCBI36
NG_008852.2:g.87285_87286delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27079_653-27078delinsGC MANE Select	ENSP00000303830.4:n.653-27079_653-27078delinsGC
ENST00000302850.9:c.653-27079_653-27078delinsGC	ENSP00000303830.4:n.653-27079_653-27078delinsGC
ENST00000341500.9:c.653-27079_653-27078delinsGC	ENSP00000342838.4:n.653-27079_653-27078delinsGC
ENST00000598216.1:n.628-27079_628-27078delinsGC
NM_000208.2:c.653-27079_653-27078delinsGC	NP_000199.2:n.653-27079_653-27078delinsGC
NM_000208.3:c.653-27079_653-27078delinsGC	NP_000199.2:n.653-27079_653-27078delinsGC
NM_001079817.1:c.653-27079_653-27078delinsGC	NP_001073285.1:n.653-27079_653-27078delinsGC
NM_001079817.2:c.653-27079_653-27078delinsGC	NP_001073285.1:n.653-27079_653-27078delinsGC
XM_011527988.1:c.731-27079_731-27078delinsGC	XP_011526290.1:n.731-27079_731-27078delinsGC
XM_011527989.1:c.731-27079_731-27078delinsGC	XP_011526291.1:n.731-27079_731-27078delinsGC
XM_011527988.2:c.653-27079_653-27078delinsGC	XP_011526290.2:n.653-27079_653-27078delinsGC
XM_011527989.3:c.653-27079_653-27078delinsGC	XP_011526291.2:n.653-27079_653-27078delinsGC
NM_000208.4:c.653-27079_653-27078delinsGC MANE Select	NP_000199.2:n.653-27079_653-27078delinsGC
NM_001079817.3:c.653-27079_653-27078delinsGC	NP_001073285.1:n.653-27079_653-27078delinsGC