Canonical Allele Identifier: CA2587921003

Gene: INSR

Linked Data

• gnomAD v4: 19-7117316-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117320del , CM000681.2:g.7117320del	GRCh38
NC_000019.9:g.7117331del , CM000681.1:g.7117331del	GRCh37
NC_000019.8:g.7068331del	NCBI36
NG_008852.2:g.181684del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3888del MANE Select	ENSP00000303830.4:p.Ser1297AlafsTer?
ENST00000302850.9:c.3888del	ENSP00000303830.4:p.Ser1297AlafsTer?
ENST00000341500.9:c.3852del	ENSP00000342838.4:p.Ser1285AlafsTer?
NM_000208.2:c.3888del	NP_000199.2:p.Ser1297AlafsTer?
NM_000208.3:c.3888del	NP_000199.2:p.Ser1297AlafsTer?
NM_001079817.1:c.3852del	NP_001073285.1:p.Ser1285AlafsTer?
NM_001079817.2:c.3852del	NP_001073285.1:p.Ser1285AlafsTer?
XM_011527988.1:c.3963del	XP_011526290.1:p.Ser1322AlafsTer?
XM_011527989.1:c.3927del	XP_011526291.1:p.Ser1310AlafsTer?
XM_011527988.2:c.3885del	XP_011526290.2:p.Ser1296AlafsTer?
XM_011527989.3:c.3849del	XP_011526291.2:p.Ser1284AlafsTer?
NM_000208.4:c.3888del MANE Select	NP_000199.2:p.Ser1297AlafsTer?
NM_001079817.3:c.3852del	NP_001073285.1:p.Ser1285AlafsTer?