Canonical Allele Identifier: CA2587922095

Gene: INSR

Linked Data

• gnomAD v4: 19-7125389-TCTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125391_7125393del , CM000681.2:g.7125391_7125393del	GRCh38
NC_000019.9:g.7125402_7125404del , CM000681.1:g.7125402_7125404del	GRCh37
NC_000019.8:g.7076402_7076404del	NCBI36
NG_008852.2:g.173609_173611del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3149_3151del MANE Select	ENSP00000303830.4:p.Ala1050del
ENST00000302850.9:c.3149_3151del	ENSP00000303830.4:p.Ala1050del
ENST00000341500.9:c.3113_3115del	ENSP00000342838.4:p.Ala1038del
NM_000208.2:c.3149_3151del	NP_000199.2:p.Ala1050del
NM_000208.3:c.3149_3151del	NP_000199.2:p.Ala1050del
NM_001079817.1:c.3113_3115del	NP_001073285.1:p.Ala1038del
NM_001079817.2:c.3113_3115del	NP_001073285.1:p.Ala1038del
XM_011527988.1:c.3224_3226del	XP_011526290.1:p.Ala1075del
XM_011527989.1:c.3188_3190del	XP_011526291.1:p.Ala1063del
XM_011527988.2:c.3146_3148del	XP_011526290.2:p.Ala1049del
XM_011527989.3:c.3110_3112del	XP_011526291.2:p.Ala1037del
NM_000208.4:c.3149_3151del MANE Select	NP_000199.2:p.Ala1050del
NM_001079817.3:c.3113_3115del	NP_001073285.1:p.Ala1038del