Canonical Allele Identifier: CA2587922097

Gene: INSR

Linked Data

• gnomAD v4: 19-7125403-GAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125404_7125405del , CM000681.2:g.7125404_7125405del	GRCh38
NC_000019.9:g.7125415_7125416del , CM000681.1:g.7125415_7125416del	GRCh37
NC_000019.8:g.7076415_7076416del	NCBI36
NG_008852.2:g.173596_173597del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3136_3137del MANE Select	ENSP00000303830.4:p.Ile1046GlnfsTer3
ENST00000302850.9:c.3136_3137del	ENSP00000303830.4:p.Ile1046GlnfsTer3
ENST00000341500.9:c.3100_3101del	ENSP00000342838.4:p.Ile1034GlnfsTer3
NM_000208.2:c.3136_3137del	NP_000199.2:p.Ile1046GlnfsTer3
NM_000208.3:c.3136_3137del	NP_000199.2:p.Ile1046GlnfsTer3
NM_001079817.1:c.3100_3101del	NP_001073285.1:p.Ile1034GlnfsTer3
NM_001079817.2:c.3100_3101del	NP_001073285.1:p.Ile1034GlnfsTer3
XM_011527988.1:c.3211_3212del	XP_011526290.1:p.Ile1071GlnfsTer3
XM_011527989.1:c.3175_3176del	XP_011526291.1:p.Ile1059GlnfsTer3
XM_011527988.2:c.3133_3134del	XP_011526290.2:p.Ile1045GlnfsTer3
XM_011527989.3:c.3097_3098del	XP_011526291.2:p.Ile1033GlnfsTer3
NM_000208.4:c.3136_3137del MANE Select	NP_000199.2:p.Ile1046GlnfsTer3
NM_001079817.3:c.3100_3101del	NP_001073285.1:p.Ile1034GlnfsTer3