Canonical Allele Identifier: CA993122723

Gene: INSR

Linked Data

• dbSNP Id: rs1975292434
• gnomAD v3: 19-7212058-GC-G
• gnomAD v4: 19-7212058-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212060del , CM000681.2:g.7212060del	GRCh38
NC_000019.9:g.7212071del , CM000681.1:g.7212071del	GRCh37
NC_000019.8:g.7163071del	NCBI36
NG_008852.2:g.86942del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27422del MANE Select	ENSP00000303830.4:n.653-27422del
ENST00000302850.9:c.653-27422del	ENSP00000303830.4:n.653-27422del
ENST00000341500.9:c.653-27422del	ENSP00000342838.4:n.653-27422del
ENST00000598216.1:n.628-27422del
NM_000208.2:c.653-27422del	NP_000199.2:n.653-27422del
NM_000208.3:c.653-27422del	NP_000199.2:n.653-27422del
NM_001079817.1:c.653-27422del	NP_001073285.1:n.653-27422del
NM_001079817.2:c.653-27422del	NP_001073285.1:n.653-27422del
XM_011527988.1:c.731-27422del	XP_011526290.1:n.731-27422del
XM_011527989.1:c.731-27422del	XP_011526291.1:n.731-27422del
XM_011527988.2:c.653-27422del	XP_011526290.2:n.653-27422del
XM_011527989.3:c.653-27422del	XP_011526291.2:n.653-27422del
NM_000208.4:c.653-27422del MANE Select	NP_000199.2:n.653-27422del
NM_001079817.3:c.653-27422del	NP_001073285.1:n.653-27422del