Canonical Allele Identifier: CA2320788140

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166002_7166003delinsCT , CM000681.2:g.7166002_7166003delinsCT	GRCh38
NC_000019.9:g.7166013_7166014delinsCT , CM000681.1:g.7166013_7166014delinsCT	GRCh37
NC_000019.8:g.7117013_7117014delinsCT	NCBI36
NG_008852.2:g.132998_132999delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1861+151_1861+152delinsAG MANE Select	ENSP00000303830.4:n.1861+151_1861+152deli...
ENST00000302850.9:c.1861+151_1861+152delinsAG	ENSP00000303830.4:n.1861+151_1861+152deli...
ENST00000341500.9:c.1861+151_1861+152delinsAG	ENSP00000342838.4:n.1861+151_1861+152deli...
ENST00000598216.1:n.1836+151_1836+152delinsAG
ENST00000600492.1:c.262+151_262+152delinsAG	ENSP00000473170.1:n.262+151_262+152delins...
NM_000208.2:c.1861+151_1861+152delinsAG	NP_000199.2:n.1861+151_1861+152delinsAG
NM_000208.3:c.1861+151_1861+152delinsAG	NP_000199.2:n.1861+151_1861+152delinsAG
NM_001079817.1:c.1861+151_1861+152delinsAG	NP_001073285.1:n.1861+151_1861+152delinsA...
NM_001079817.2:c.1861+151_1861+152delinsAG	NP_001073285.1:n.1861+151_1861+152delinsA...
XM_011527988.1:c.1939+151_1939+152delinsAG	XP_011526290.1:n.1939+151_1939+152delinsA...
XM_011527989.1:c.1939+151_1939+152delinsAG	XP_011526291.1:n.1939+151_1939+152delinsA...
XM_011527988.2:c.1861+151_1861+152delinsAG	XP_011526290.2:n.1861+151_1861+152delinsA...
XM_011527989.3:c.1861+151_1861+152delinsAG	XP_011526291.2:n.1861+151_1861+152delinsA...
NM_000208.4:c.1861+151_1861+152delinsAG MANE Select	NP_000199.2:n.1861+151_1861+152delinsAG
NM_001079817.3:c.1861+151_1861+152delinsAG	NP_001073285.1:n.1861+151_1861+152delinsA...