Canonical Allele Identifier: CA2320788155

Gene: INSR

Linked Data

• dbSNP Id: rs1973880663

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166032_7166033insG , CM000681.2:g.7166032_7166033insG	GRCh38
NC_000019.9:g.7166043_7166044insG , CM000681.1:g.7166043_7166044insG	GRCh37
NC_000019.8:g.7117043_7117044insG	NCBI36
NG_008852.2:g.132968_132969insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1861+121_1861+122insC MANE Select	ENSP00000303830.4:n.1861+121_1861+122insC
ENST00000302850.9:c.1861+121_1861+122insC	ENSP00000303830.4:n.1861+121_1861+122insC
ENST00000341500.9:c.1861+121_1861+122insC	ENSP00000342838.4:n.1861+121_1861+122insC
ENST00000598216.1:n.1836+121_1836+122insC
ENST00000600492.1:c.262+121_262+122insC	ENSP00000473170.1:n.262+121_262+122insC
NM_000208.2:c.1861+121_1861+122insC	NP_000199.2:n.1861+121_1861+122insC
NM_000208.3:c.1861+121_1861+122insC	NP_000199.2:n.1861+121_1861+122insC
NM_001079817.1:c.1861+121_1861+122insC	NP_001073285.1:n.1861+121_1861+122insC
NM_001079817.2:c.1861+121_1861+122insC	NP_001073285.1:n.1861+121_1861+122insC
XM_011527988.1:c.1939+121_1939+122insC	XP_011526290.1:n.1939+121_1939+122insC
XM_011527989.1:c.1939+121_1939+122insC	XP_011526291.1:n.1939+121_1939+122insC
XM_011527988.2:c.1861+121_1861+122insC	XP_011526290.2:n.1861+121_1861+122insC
XM_011527989.3:c.1861+121_1861+122insC	XP_011526291.2:n.1861+121_1861+122insC
NM_000208.4:c.1861+121_1861+122insC MANE Select	NP_000199.2:n.1861+121_1861+122insC
NM_001079817.3:c.1861+121_1861+122insC	NP_001073285.1:n.1861+121_1861+122insC