Canonical Allele Identifier: CA304866449

Gene: INSR

Linked Data

• dbSNP Id: rs763298176
• MyVariant Identifiers: chr19:g.7117190_7117191insC (hg19) ; chr19:g.7117179_7117180insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117185dup , CM000681.2:g.7117185dup	GRCh38
NC_000019.9:g.7117196dup , CM000681.1:g.7117196dup	GRCh37
NC_000019.8:g.7068196dup	NCBI36
NG_008852.2:g.181821dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4025dup MANE Select	ENSP00000303830.4:p.Arg1343ProfsTer?
ENST00000302850.9:c.4025dup	ENSP00000303830.4:p.Arg1343ProfsTer?
ENST00000341500.9:c.3989dup	ENSP00000342838.4:p.Arg1331ProfsTer?
NM_000208.2:c.4025dup	NP_000199.2:p.Arg1343ProfsTer?
NM_000208.3:c.4025dup	NP_000199.2:p.Arg1343ProfsTer?
NM_001079817.1:c.3989dup	NP_001073285.1:p.Arg1331ProfsTer?
NM_001079817.2:c.3989dup	NP_001073285.1:p.Arg1331ProfsTer?
XM_011527988.1:c.4100dup	XP_011526290.1:p.Arg1368ProfsTer?
XM_011527989.1:c.4064dup	XP_011526291.1:p.Arg1356ProfsTer?
XM_011527988.2:c.4022dup	XP_011526290.2:p.Arg1342ProfsTer?
XM_011527989.3:c.3986dup	XP_011526291.2:p.Arg1330ProfsTer?
NM_000208.4:c.4025dup MANE Select	NP_000199.2:p.Arg1343ProfsTer?
NM_001079817.3:c.3989dup	NP_001073285.1:p.Arg1331ProfsTer?