Canonical Allele Identifier: CA2587925215

Gene: INSR

Linked Data

• gnomAD v4: 19-7166304-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166308del , CM000681.2:g.7166308del	GRCh38
NC_000019.9:g.7166319del , CM000681.1:g.7166319del	GRCh37
NC_000019.8:g.7117319del	NCBI36
NG_008852.2:g.132696del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1710del MANE Select	ENSP00000303830.4:p.Lys571AsnfsTer9
ENST00000302850.9:c.1710del	ENSP00000303830.4:p.Lys571AsnfsTer9
ENST00000341500.9:c.1710del	ENSP00000342838.4:p.Lys571AsnfsTer9
ENST00000598216.1:n.1685del
ENST00000600492.1:c.111del	ENSP00000473170.1:p.Lys38AsnfsTer9
NM_000208.2:c.1710del	NP_000199.2:p.Lys571AsnfsTer9
NM_000208.3:c.1710del	NP_000199.2:p.Lys571AsnfsTer9
NM_001079817.1:c.1710del	NP_001073285.1:p.Lys571AsnfsTer9
NM_001079817.2:c.1710del	NP_001073285.1:p.Lys571AsnfsTer9
XM_011527988.1:c.1788del	XP_011526290.1:p.Lys597AsnfsTer9
XM_011527989.1:c.1788del	XP_011526291.1:p.Lys597AsnfsTer9
XM_011527988.2:c.1710del	XP_011526290.2:p.Lys571AsnfsTer9
XM_011527989.3:c.1710del	XP_011526291.2:p.Lys571AsnfsTer9
NM_000208.4:c.1710del MANE Select	NP_000199.2:p.Lys571AsnfsTer9
NM_001079817.3:c.1710del	NP_001073285.1:p.Lys571AsnfsTer9