Canonical Allele Identifier: CA2587923309

Gene: INSR

Linked Data

• gnomAD v4: 19-7142982-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7142984del , CM000681.2:g.7142984del	GRCh38
NC_000019.9:g.7142995del , CM000681.1:g.7142995del	GRCh37
NC_000019.8:g.7093995del	NCBI36
NG_008852.2:g.156018del

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2375del MANE Select	ENSP00000303830.4:p.Pro792ArgfsTer11
ENST00000302850.9:c.2375del	ENSP00000303830.4:p.Pro792ArgfsTer11
ENST00000341500.9:c.2339del	ENSP00000342838.4:p.Pro780ArgfsTer11
ENST00000597211.1:n.58del
NM_000208.2:c.2375del	NP_000199.2:p.Pro792ArgfsTer11
NM_000208.3:c.2375del	NP_000199.2:p.Pro792ArgfsTer11
NM_001079817.1:c.2339del	NP_001073285.1:p.Pro780ArgfsTer11
NM_001079817.2:c.2339del	NP_001073285.1:p.Pro780ArgfsTer11
XM_011527988.1:c.2453del	XP_011526290.1:p.Pro818ArgfsTer11
XM_011527989.1:c.2417del	XP_011526291.1:p.Pro806ArgfsTer11
XM_011527988.2:c.2375del	XP_011526290.2:p.Pro792ArgfsTer11
XM_011527989.3:c.2339del	XP_011526291.2:p.Pro780ArgfsTer11
NM_000208.4:c.2375del MANE Select	NP_000199.2:p.Pro792ArgfsTer11
NM_001079817.3:c.2339del	NP_001073285.1:p.Pro780ArgfsTer11