Canonical Allele Identifier: CA2587922648

Gene: INSR

Linked Data

• gnomAD v4: 19-7132018-AAGCACCGCAGCAGCTGATAGGCCTGAGAGTCAAGGCCAGGGCC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132025_7132067del , CM000681.2:g.7132025_7132067del	GRCh38
NC_000019.9:g.7132036_7132078del , CM000681.1:g.7132036_7132078del	GRCh37
NC_000019.8:g.7083036_7083078del	NCBI36
NG_008852.2:g.166940_166982del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2842+97_2842+139del MANE Select	ENSP00000303830.4:n.2842+97_2842+139del
ENST00000302850.9:c.2842+97_2842+139del	ENSP00000303830.4:n.2842+97_2842+139del
ENST00000341500.9:c.2806+97_2806+139del	ENSP00000342838.4:n.2806+97_2806+139del
NM_000208.2:c.2842+97_2842+139del	NP_000199.2:n.2842+97_2842+139del
NM_000208.3:c.2842+97_2842+139del	NP_000199.2:n.2842+97_2842+139del
NM_001079817.1:c.2806+97_2806+139del	NP_001073285.1:n.2806+97_2806+139del
NM_001079817.2:c.2806+97_2806+139del	NP_001073285.1:n.2806+97_2806+139del
XM_011527988.1:c.2920+97_2920+139del	XP_011526290.1:n.2920+97_2920+139del
XM_011527989.1:c.2884+97_2884+139del	XP_011526291.1:n.2884+97_2884+139del
XM_011527988.2:c.2842+97_2842+139del	XP_011526290.2:n.2842+97_2842+139del
XM_011527989.3:c.2806+97_2806+139del	XP_011526291.2:n.2806+97_2806+139del
NM_000208.4:c.2842+97_2842+139del MANE Select	NP_000199.2:n.2842+97_2842+139del
NM_001079817.3:c.2806+97_2806+139del	NP_001073285.1:n.2806+97_2806+139del