Canonical Allele Identifier: CA505400111

Gene: INSR

Linked Data

• COSMIC: COSM1167675 ; COSM1167676
• MyVariant Identifiers: chr19:g.7117320del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117310del , CM000681.2:g.7117310del	GRCh38
NC_000019.9:g.7117321del , CM000681.1:g.7117321del	GRCh37
NC_000019.8:g.7068321del	NCBI36
NG_008852.2:g.181692del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3896del MANE Select	ENSP00000303830.4:p.Pro1299GlnfsTer?
ENST00000302850.9:c.3896del	ENSP00000303830.4:p.Pro1299GlnfsTer?
ENST00000341500.9:c.3860del	ENSP00000342838.4:p.Pro1287GlnfsTer?
NM_000208.2:c.3896del	NP_000199.2:p.Pro1299GlnfsTer?
NM_000208.3:c.3896del	NP_000199.2:p.Pro1299GlnfsTer?
NM_001079817.1:c.3860del	NP_001073285.1:p.Pro1287GlnfsTer?
NM_001079817.2:c.3860del	NP_001073285.1:p.Pro1287GlnfsTer?
XM_011527988.1:c.3971del	XP_011526290.1:p.Pro1324GlnfsTer?
XM_011527989.1:c.3935del	XP_011526291.1:p.Pro1312GlnfsTer?
XM_011527988.2:c.3893del	XP_011526290.2:p.Pro1298GlnfsTer?
XM_011527989.3:c.3857del	XP_011526291.2:p.Pro1286GlnfsTer?
NM_000208.4:c.3896del MANE Select	NP_000199.2:p.Pro1299GlnfsTer?
NM_001079817.3:c.3860del	NP_001073285.1:p.Pro1287GlnfsTer?