Canonical Allele Identifier: CA2587925449

Gene: INSR

Linked Data

• gnomAD v4: 19-7172179-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172182del , CM000681.2:g.7172182del	GRCh38
NC_000019.9:g.7172193del , CM000681.1:g.7172193del	GRCh37
NC_000019.8:g.7123193del	NCBI36
NG_008852.2:g.126821del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1268+110del MANE Select	ENSP00000303830.4:n.1268+110del
ENST00000302850.9:c.1268+110del	ENSP00000303830.4:n.1268+110del
ENST00000341500.9:c.1268+110del	ENSP00000342838.4:n.1268+110del
ENST00000598216.1:n.1243+110del
NM_000208.2:c.1268+110del	NP_000199.2:n.1268+110del
NM_000208.3:c.1268+110del	NP_000199.2:n.1268+110del
NM_001079817.1:c.1268+110del	NP_001073285.1:n.1268+110del
NM_001079817.2:c.1268+110del	NP_001073285.1:n.1268+110del
XM_011527988.1:c.1346+110del	XP_011526290.1:n.1346+110del
XM_011527989.1:c.1346+110del	XP_011526291.1:n.1346+110del
XM_011527988.2:c.1268+110del	XP_011526290.2:n.1268+110del
XM_011527989.3:c.1268+110del	XP_011526291.2:n.1268+110del
NM_000208.4:c.1268+110del MANE Select	NP_000199.2:n.1268+110del
NM_001079817.3:c.1268+110del	NP_001073285.1:n.1268+110del