Canonical Allele Identifier: CA2320796082

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184288_7184289delinsGC , CM000681.2:g.7184288_7184289delinsGC	GRCh38
NC_000019.9:g.7184299_7184300delinsGC , CM000681.1:g.7184299_7184300delinsGC	GRCh37
NC_000019.8:g.7135299_7135300delinsGC	NCBI36
NG_008852.2:g.114712_114713delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.974+27_974+28delinsGC MANE Select	ENSP00000303830.4:n.974+27_974+28delinsGC...
ENST00000302850.9:c.974+27_974+28delinsGC	ENSP00000303830.4:n.974+27_974+28delinsGC...
ENST00000341500.9:c.974+27_974+28delinsGC	ENSP00000342838.4:n.974+27_974+28delinsGC...
ENST00000598216.1:n.949+27_949+28delinsGC
NM_000208.2:c.974+27_974+28delinsGC	NP_000199.2:n.974+27_974+28delinsGC
NM_000208.3:c.974+27_974+28delinsGC	NP_000199.2:n.974+27_974+28delinsGC
NM_001079817.1:c.974+27_974+28delinsGC	NP_001073285.1:n.974+27_974+28delinsGC
NM_001079817.2:c.974+27_974+28delinsGC	NP_001073285.1:n.974+27_974+28delinsGC
XM_011527988.1:c.1052+27_1052+28delinsGC	XP_011526290.1:n.1052+27_1052+28delinsGC
XM_011527989.1:c.1052+27_1052+28delinsGC	XP_011526291.1:n.1052+27_1052+28delinsGC
XM_011527988.2:c.974+27_974+28delinsGC	XP_011526290.2:n.974+27_974+28delinsGC
XM_011527989.3:c.974+27_974+28delinsGC	XP_011526291.2:n.974+27_974+28delinsGC
NM_000208.4:c.974+27_974+28delinsGC MANE Select	NP_000199.2:n.974+27_974+28delinsGC
NM_001079817.3:c.974+27_974+28delinsGC	NP_001073285.1:n.974+27_974+28delinsGC