Canonical Allele Identifier: CA2587925142

Gene: INSR

Linked Data

• gnomAD v4: 19-7166041-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166041_7166042insG , CM000681.2:g.7166041_7166042insG	GRCh38
NC_000019.9:g.7166052_7166053insG , CM000681.1:g.7166052_7166053insG	GRCh37
NC_000019.8:g.7117052_7117053insG	NCBI36
NG_008852.2:g.132959_132960insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+112_1861+113insC MANE Select	ENSP00000303830.4:n.1861+112_1861+113insC
ENST00000302850.9:c.1861+112_1861+113insC	ENSP00000303830.4:n.1861+112_1861+113insC
ENST00000341500.9:c.1861+112_1861+113insC	ENSP00000342838.4:n.1861+112_1861+113insC
ENST00000598216.1:n.1836+112_1836+113insC
ENST00000600492.1:c.262+112_262+113insC	ENSP00000473170.1:n.262+112_262+113insC
NM_000208.2:c.1861+112_1861+113insC	NP_000199.2:n.1861+112_1861+113insC
NM_000208.3:c.1861+112_1861+113insC	NP_000199.2:n.1861+112_1861+113insC
NM_001079817.1:c.1861+112_1861+113insC	NP_001073285.1:n.1861+112_1861+113insC
NM_001079817.2:c.1861+112_1861+113insC	NP_001073285.1:n.1861+112_1861+113insC
XM_011527988.1:c.1939+112_1939+113insC	XP_011526290.1:n.1939+112_1939+113insC
XM_011527989.1:c.1939+112_1939+113insC	XP_011526291.1:n.1939+112_1939+113insC
XM_011527988.2:c.1861+112_1861+113insC	XP_011526290.2:n.1861+112_1861+113insC
XM_011527989.3:c.1861+112_1861+113insC	XP_011526291.2:n.1861+112_1861+113insC
NM_000208.4:c.1861+112_1861+113insC MANE Select	NP_000199.2:n.1861+112_1861+113insC
NM_001079817.3:c.1861+112_1861+113insC	NP_001073285.1:n.1861+112_1861+113insC