Canonical Allele Identifier: CA2813462927

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125362_7125364del , CM000681.2:g.7125362_7125364del	GRCh38
NC_000019.9:g.7125373_7125375del , CM000681.1:g.7125373_7125375del	GRCh37
NC_000019.8:g.7076373_7076375del	NCBI36
NG_008852.2:g.173638_173640del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3178_3180del MANE Select	ENSP00000303830.4:p.Asn1060del
ENST00000302850.9:c.3178_3180del	ENSP00000303830.4:p.Asn1060del
ENST00000341500.9:c.3142_3144del	ENSP00000342838.4:p.Asn1048del
ENST00000593970.1:n.24_26del
NM_000208.2:c.3178_3180del	NP_000199.2:p.Asn1060del
NM_000208.3:c.3178_3180del	NP_000199.2:p.Asn1060del
NM_001079817.1:c.3142_3144del	NP_001073285.1:p.Asn1048del
NM_001079817.2:c.3142_3144del	NP_001073285.1:p.Asn1048del
XM_011527988.1:c.3253_3255del	XP_011526290.1:p.Asn1085del
XM_011527989.1:c.3217_3219del	XP_011526291.1:p.Asn1073del
XM_011527988.2:c.3175_3177del	XP_011526290.2:p.Asn1059del
XM_011527989.3:c.3139_3141del	XP_011526291.2:p.Asn1047del
NM_000208.4:c.3178_3180del MANE Select	NP_000199.2:p.Asn1060del
NM_001079817.3:c.3142_3144del	NP_001073285.1:p.Asn1048del