Canonical Allele Identifier: CA2320788077

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7165865_7165866delinsAG , CM000681.2:g.7165865_7165866delinsAG	GRCh38
NC_000019.9:g.7165876_7165877delinsAG , CM000681.1:g.7165876_7165877delinsAG	GRCh37
NC_000019.8:g.7116876_7116877delinsAG	NCBI36
NG_008852.2:g.133135_133136delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+288_1861+289delinsCT MANE Select	ENSP00000303830.4:n.1861+288_1861+289delinsCT
ENST00000302850.9:c.1861+288_1861+289delinsCT	ENSP00000303830.4:n.1861+288_1861+289delinsCT
ENST00000341500.9:c.1861+288_1861+289delinsCT	ENSP00000342838.4:n.1861+288_1861+289delinsCT
ENST00000598216.1:n.1836+288_1836+289delinsCT
ENST00000600492.1:c.262+288_262+289delinsCT	ENSP00000473170.1:n.262+288_262+289delinsCT
NM_000208.2:c.1861+288_1861+289delinsCT	NP_000199.2:n.1861+288_1861+289delinsCT
NM_000208.3:c.1861+288_1861+289delinsCT	NP_000199.2:n.1861+288_1861+289delinsCT
NM_001079817.1:c.1861+288_1861+289delinsCT	NP_001073285.1:n.1861+288_1861+289delinsCT
NM_001079817.2:c.1861+288_1861+289delinsCT	NP_001073285.1:n.1861+288_1861+289delinsCT
XM_011527988.1:c.1939+288_1939+289delinsCT	XP_011526290.1:n.1939+288_1939+289delinsCT
XM_011527989.1:c.1939+288_1939+289delinsCT	XP_011526291.1:n.1939+288_1939+289delinsCT
XM_011527988.2:c.1861+288_1861+289delinsCT	XP_011526290.2:n.1861+288_1861+289delinsCT
XM_011527989.3:c.1861+288_1861+289delinsCT	XP_011526291.2:n.1861+288_1861+289delinsCT
NM_000208.4:c.1861+288_1861+289delinsCT MANE Select	NP_000199.2:n.1861+288_1861+289delinsCT
NM_001079817.3:c.1861+288_1861+289delinsCT	NP_001073285.1:n.1861+288_1861+289delinsCT