Canonical Allele Identifier: CA2320788113

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7165945_7165946delinsCT , CM000681.2:g.7165945_7165946delinsCT	GRCh38
NC_000019.9:g.7165956_7165957delinsCT , CM000681.1:g.7165956_7165957delinsCT	GRCh37
NC_000019.8:g.7116956_7116957delinsCT	NCBI36
NG_008852.2:g.133055_133056delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+208_1861+209delinsAG MANE Select	ENSP00000303830.4:n.1861+208_1861+209delinsAG
ENST00000302850.9:c.1861+208_1861+209delinsAG	ENSP00000303830.4:n.1861+208_1861+209delinsAG
ENST00000341500.9:c.1861+208_1861+209delinsAG	ENSP00000342838.4:n.1861+208_1861+209delinsAG
ENST00000598216.1:n.1836+208_1836+209delinsAG
ENST00000600492.1:c.262+208_262+209delinsAG	ENSP00000473170.1:n.262+208_262+209delinsAG
NM_000208.2:c.1861+208_1861+209delinsAG	NP_000199.2:n.1861+208_1861+209delinsAG
NM_000208.3:c.1861+208_1861+209delinsAG	NP_000199.2:n.1861+208_1861+209delinsAG
NM_001079817.1:c.1861+208_1861+209delinsAG	NP_001073285.1:n.1861+208_1861+209delinsAG
NM_001079817.2:c.1861+208_1861+209delinsAG	NP_001073285.1:n.1861+208_1861+209delinsAG
XM_011527988.1:c.1939+208_1939+209delinsAG	XP_011526290.1:n.1939+208_1939+209delinsAG
XM_011527989.1:c.1939+208_1939+209delinsAG	XP_011526291.1:n.1939+208_1939+209delinsAG
XM_011527988.2:c.1861+208_1861+209delinsAG	XP_011526290.2:n.1861+208_1861+209delinsAG
XM_011527989.3:c.1861+208_1861+209delinsAG	XP_011526291.2:n.1861+208_1861+209delinsAG
NM_000208.4:c.1861+208_1861+209delinsAG MANE Select	NP_000199.2:n.1861+208_1861+209delinsAG
NM_001079817.3:c.1861+208_1861+209delinsAG	NP_001073285.1:n.1861+208_1861+209delinsAG