Canonical Allele Identifier: CA2320788165

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166051_7166053delinsAAT , CM000681.2:g.7166051_7166053delinsAAT	GRCh38
NC_000019.9:g.7166062_7166064delinsAAT , CM000681.1:g.7166062_7166064delinsAAT	GRCh37
NC_000019.8:g.7117062_7117064delinsAAT	NCBI36
NG_008852.2:g.132948_132950delinsATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+101_1861+103delinsATT MANE Select	ENSP00000303830.4:n.1861+101_1861+103delinsATT
ENST00000302850.9:c.1861+101_1861+103delinsATT	ENSP00000303830.4:n.1861+101_1861+103delinsATT
ENST00000341500.9:c.1861+101_1861+103delinsATT	ENSP00000342838.4:n.1861+101_1861+103delinsATT
ENST00000598216.1:n.1836+101_1836+103delinsATT
ENST00000600492.1:c.262+101_262+103delinsATT	ENSP00000473170.1:n.262+101_262+103delinsATT
NM_000208.2:c.1861+101_1861+103delinsATT	NP_000199.2:n.1861+101_1861+103delinsATT
NM_000208.3:c.1861+101_1861+103delinsATT	NP_000199.2:n.1861+101_1861+103delinsATT
NM_001079817.1:c.1861+101_1861+103delinsATT	NP_001073285.1:n.1861+101_1861+103delinsATT
NM_001079817.2:c.1861+101_1861+103delinsATT	NP_001073285.1:n.1861+101_1861+103delinsATT
XM_011527988.1:c.1939+101_1939+103delinsATT	XP_011526290.1:n.1939+101_1939+103delinsATT
XM_011527989.1:c.1939+101_1939+103delinsATT	XP_011526291.1:n.1939+101_1939+103delinsATT
XM_011527988.2:c.1861+101_1861+103delinsATT	XP_011526290.2:n.1861+101_1861+103delinsATT
XM_011527989.3:c.1861+101_1861+103delinsATT	XP_011526291.2:n.1861+101_1861+103delinsATT
NM_000208.4:c.1861+101_1861+103delinsATT MANE Select	NP_000199.2:n.1861+101_1861+103delinsATT
NM_001079817.3:c.1861+101_1861+103delinsATT	NP_001073285.1:n.1861+101_1861+103delinsATT