Canonical Allele Identifier: CA2320796116

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184360_7184363delinsCTTG , CM000681.2:g.7184360_7184363delinsCTTG	GRCh38
NC_000019.9:g.7184371_7184374delinsCTTG , CM000681.1:g.7184371_7184374delinsCTTG	GRCh37
NC_000019.8:g.7135371_7135374delinsCTTG	NCBI36
NG_008852.2:g.114638_114641delinsCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.927_930delinsCAAG MANE Select	ENSP00000303830.4:p.Asn309=
ENST00000302850.9:c.927_930delinsCAAG	ENSP00000303830.4:p.Asn309=
ENST00000341500.9:c.927_930delinsCAAG	ENSP00000342838.4:p.Asn309=
ENST00000598216.1:n.902_905delinsCAAG
NM_000208.2:c.927_930delinsCAAG	NP_000199.2:p.Asn309=
NM_000208.3:c.927_930delinsCAAG	NP_000199.2:p.Asn309=
NM_001079817.1:c.927_930delinsCAAG	NP_001073285.1:p.Asn309=
NM_001079817.2:c.927_930delinsCAAG	NP_001073285.1:p.Asn309=
XM_011527988.1:c.1005_1008delinsCAAG	XP_011526290.1:p.Asn335=
XM_011527989.1:c.1005_1008delinsCAAG	XP_011526291.1:p.Asn335=
XM_011527988.2:c.927_930delinsCAAG	XP_011526290.2:p.Asn309=
XM_011527989.3:c.927_930delinsCAAG	XP_011526291.2:p.Asn309=
NM_000208.4:c.927_930delinsCAAG MANE Select	NP_000199.2:p.Asn309=
NM_001079817.3:c.927_930delinsCAAG	NP_001073285.1:p.Asn309=