Canonical Allele Identifier: CA920049205

Gene: INSR

Linked Data

• dbSNP Id: rs1555743277
• gnomAD v4: 19-7166051-AAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166053_7166054del , CM000681.2:g.7166053_7166054del	GRCh38
NC_000019.9:g.7166064_7166065del , CM000681.1:g.7166064_7166065del	GRCh37
NC_000019.8:g.7117064_7117065del	NCBI36
NG_008852.2:g.132948_132949del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+101_1861+102del MANE Select	ENSP00000303830.4:n.1861+101_1861+102del
ENST00000302850.9:c.1861+101_1861+102del	ENSP00000303830.4:n.1861+101_1861+102del
ENST00000341500.9:c.1861+101_1861+102del	ENSP00000342838.4:n.1861+101_1861+102del
ENST00000598216.1:n.1836+101_1836+102del
ENST00000600492.1:c.262+101_262+102del	ENSP00000473170.1:n.262+101_262+102del
NM_000208.2:c.1861+101_1861+102del	NP_000199.2:n.1861+101_1861+102del
NM_000208.3:c.1861+101_1861+102del	NP_000199.2:n.1861+101_1861+102del
NM_001079817.1:c.1861+101_1861+102del	NP_001073285.1:n.1861+101_1861+102del
NM_001079817.2:c.1861+101_1861+102del	NP_001073285.1:n.1861+101_1861+102del
XM_011527988.1:c.1939+101_1939+102del	XP_011526290.1:n.1939+101_1939+102del
XM_011527989.1:c.1939+101_1939+102del	XP_011526291.1:n.1939+101_1939+102del
XM_011527988.2:c.1861+101_1861+102del	XP_011526290.2:n.1861+101_1861+102del
XM_011527989.3:c.1861+101_1861+102del	XP_011526291.2:n.1861+101_1861+102del
NM_000208.4:c.1861+101_1861+102del MANE Select	NP_000199.2:n.1861+101_1861+102del
NM_001079817.3:c.1861+101_1861+102del	NP_001073285.1:n.1861+101_1861+102del