Canonical Allele Identifier: CA2813449709

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166031_7166032insG , CM000681.2:g.7166031_7166032insG	GRCh38
NC_000019.9:g.7166042_7166043insG , CM000681.1:g.7166042_7166043insG	GRCh37
NC_000019.8:g.7117042_7117043insG	NCBI36
NG_008852.2:g.132969_132970insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1861+122_1861+123insC MANE Select	ENSP00000303830.4:n.1861+122_1861+123insC
ENST00000302850.9:c.1861+122_1861+123insC	ENSP00000303830.4:n.1861+122_1861+123insC
ENST00000341500.9:c.1861+122_1861+123insC	ENSP00000342838.4:n.1861+122_1861+123insC
ENST00000598216.1:n.1836+122_1836+123insC
ENST00000600492.1:c.262+122_262+123insC	ENSP00000473170.1:n.262+122_262+123insC
NM_000208.2:c.1861+122_1861+123insC	NP_000199.2:n.1861+122_1861+123insC
NM_000208.3:c.1861+122_1861+123insC	NP_000199.2:n.1861+122_1861+123insC
NM_001079817.1:c.1861+122_1861+123insC	NP_001073285.1:n.1861+122_1861+123insC
NM_001079817.2:c.1861+122_1861+123insC	NP_001073285.1:n.1861+122_1861+123insC
XM_011527988.1:c.1939+122_1939+123insC	XP_011526290.1:n.1939+122_1939+123insC
XM_011527989.1:c.1939+122_1939+123insC	XP_011526291.1:n.1939+122_1939+123insC
XM_011527988.2:c.1861+122_1861+123insC	XP_011526290.2:n.1861+122_1861+123insC
XM_011527989.3:c.1861+122_1861+123insC	XP_011526291.2:n.1861+122_1861+123insC
NM_000208.4:c.1861+122_1861+123insC MANE Select	NP_000199.2:n.1861+122_1861+123insC
NM_001079817.3:c.1861+122_1861+123insC	NP_001073285.1:n.1861+122_1861+123insC