Canonical Allele Identifier: CA403668245

Gene: INSR

Linked Data

• COSMIC: COSM4931109 ; COSM4931110
• MyVariant Identifiers: chr19:g.7117093T>A (hg19) ; chr19:g.7117082T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117082T>A , CM000681.2:g.7117082T>A	GRCh38
NC_000019.9:g.7117093T>A , CM000681.1:g.7117093T>A	GRCh37
NC_000019.8:g.7068093T>A	NCBI36
NG_008852.2:g.181919A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4123A>T MANE Select	ENSP00000303830.4:p.Thr1375Ser
ENST00000302850.9:c.4123A>T	ENSP00000303830.4:p.Thr1375Ser
ENST00000341500.9:c.4087A>T	ENSP00000342838.4:p.Thr1363Ser
NM_000208.2:c.4123A>T	NP_000199.2:p.Thr1375Ser
NM_000208.3:c.4123A>T	NP_000199.2:p.Thr1375Ser
NM_001079817.1:c.4087A>T	NP_001073285.1:p.Thr1363Ser
NM_001079817.2:c.4087A>T	NP_001073285.1:p.Thr1363Ser
XM_011527988.1:c.4198A>T	XP_011526290.1:p.Thr1400Ser
XM_011527989.1:c.4162A>T	XP_011526291.1:p.Thr1388Ser
XM_011527988.2:c.4120A>T	XP_011526290.2:p.Thr1374Ser
XM_011527989.3:c.4084A>T	XP_011526291.2:p.Thr1362Ser
NM_000208.4:c.4123A>T MANE Select	NP_000199.2:p.Thr1375Ser
NM_001079817.3:c.4087A>T	NP_001073285.1:p.Thr1363Ser