Canonical Allele Identifier: CA2587922674

Gene: INSR

Linked Data

• gnomAD v4: 19-7132042-TGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132046_7132047del , CM000681.2:g.7132046_7132047del	GRCh38
NC_000019.9:g.7132057_7132058del , CM000681.1:g.7132057_7132058del	GRCh37
NC_000019.8:g.7083057_7083058del	NCBI36
NG_008852.2:g.166957_166958del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2842+114_2842+115del MANE Select	ENSP00000303830.4:n.2842+114_2842+115del
ENST00000302850.9:c.2842+114_2842+115del	ENSP00000303830.4:n.2842+114_2842+115del
ENST00000341500.9:c.2806+114_2806+115del	ENSP00000342838.4:n.2806+114_2806+115del
NM_000208.2:c.2842+114_2842+115del	NP_000199.2:n.2842+114_2842+115del
NM_000208.3:c.2842+114_2842+115del	NP_000199.2:n.2842+114_2842+115del
NM_001079817.1:c.2806+114_2806+115del	NP_001073285.1:n.2806+114_2806+115del
NM_001079817.2:c.2806+114_2806+115del	NP_001073285.1:n.2806+114_2806+115del
XM_011527988.1:c.2920+114_2920+115del	XP_011526290.1:n.2920+114_2920+115del
XM_011527989.1:c.2884+114_2884+115del	XP_011526291.1:n.2884+114_2884+115del
XM_011527988.2:c.2842+114_2842+115del	XP_011526290.2:n.2842+114_2842+115del
XM_011527989.3:c.2806+114_2806+115del	XP_011526291.2:n.2806+114_2806+115del
NM_000208.4:c.2842+114_2842+115del MANE Select	NP_000199.2:n.2842+114_2842+115del
NM_001079817.3:c.2806+114_2806+115del	NP_001073285.1:n.2806+114_2806+115del