Canonical Allele Identifier: CA920049000

Gene: INSR

Linked Data

• dbSNP Id: rs1568423965
• gnomAD v4: 19-7117070-A-AC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117072dup , CM000681.2:g.7117072dup	GRCh38
NC_000019.9:g.7117083dup , CM000681.1:g.7117083dup	GRCh37
NC_000019.8:g.7068083dup	NCBI36
NG_008852.2:g.181930dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4134dup MANE Select	ENSP00000303830.4:p.Ser1379ValfsTer25
ENST00000302850.9:c.4134dup	ENSP00000303830.4:p.Ser1379ValfsTer25
ENST00000341500.9:c.4098dup	ENSP00000342838.4:p.Ser1367ValfsTer25
NM_000208.2:c.4134dup	NP_000199.2:p.Ser1379ValfsTer25
NM_000208.3:c.4134dup	NP_000199.2:p.Ser1379ValfsTer25
NM_001079817.1:c.4098dup	NP_001073285.1:p.Ser1367ValfsTer25
NM_001079817.2:c.4098dup	NP_001073285.1:p.Ser1367ValfsTer25
XM_011527988.1:c.4209dup	XP_011526290.1:p.Ser1404ValfsTer25
XM_011527989.1:c.4173dup	XP_011526291.1:p.Ser1392ValfsTer25
XM_011527988.2:c.4131dup	XP_011526290.2:p.Ser1378ValfsTer25
XM_011527989.3:c.4095dup	XP_011526291.2:p.Ser1366ValfsTer25
NM_000208.4:c.4134dup MANE Select	NP_000199.2:p.Ser1379ValfsTer25
NM_001079817.3:c.4098dup	NP_001073285.1:p.Ser1367ValfsTer25