Canonical Allele Identifier: CA2320836491

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7267643_7267647delinsGTAGT , CM000681.2:g.7267643_7267647delinsGTAGT	GRCh38
NC_000019.9:g.7267654_7267658delinsGTAGT , CM000681.1:g.7267654_7267658delinsGTAGT	GRCh37
NC_000019.8:g.7218654_7218658delinsGTAGT	NCBI36
NG_008852.2:g.31354_31358delinsACTAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.350_354delinsACTAC MANE Select	ENSP00000303830.4:p.Asn117=
ENST00000302850.9:c.350_354delinsACTAC	ENSP00000303830.4:p.Asn117=
ENST00000341500.9:c.350_354delinsACTAC	ENSP00000342838.4:p.Asn117=
ENST00000598216.1:n.325_329delinsACTAC
NM_000208.2:c.350_354delinsACTAC	NP_000199.2:p.Asn117=
NM_000208.3:c.350_354delinsACTAC	NP_000199.2:p.Asn117=
NM_001079817.1:c.350_354delinsACTAC	NP_001073285.1:p.Asn117=
NM_001079817.2:c.350_354delinsACTAC	NP_001073285.1:p.Asn117=
XM_011527988.1:c.428_432delinsACTAC	XP_011526290.1:p.Asn143=
XM_011527989.1:c.428_432delinsACTAC	XP_011526291.1:p.Asn143=
XM_011527988.2:c.350_354delinsACTAC	XP_011526290.2:p.Asn117=
XM_011527989.3:c.350_354delinsACTAC	XP_011526291.2:p.Asn117=
NM_000208.4:c.350_354delinsACTAC MANE Select	NP_000199.2:p.Asn117=
NM_001079817.3:c.350_354delinsACTAC	NP_001073285.1:p.Asn117=