Canonical Allele Identifier: CA505400140

Gene: INSR

Linked Data

• COSMIC: COSM1722087 ; COSM1722088
• MyVariant Identifiers: chr19:g.7117367G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117356G>A , CM000681.2:g.7117356G>A	GRCh38
NC_000019.9:g.7117367G>A , CM000681.1:g.7117367G>A	GRCh37
NC_000019.8:g.7068367G>A	NCBI36
NG_008852.2:g.181645C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3849C>T MANE Select	ENSP00000303830.4:p.Phe1283=
ENST00000302850.9:c.3849C>T	ENSP00000303830.4:p.Phe1283=
ENST00000341500.9:c.3813C>T	ENSP00000342838.4:p.Phe1271=
NM_000208.2:c.3849C>T	NP_000199.2:p.Phe1283=
NM_000208.3:c.3849C>T	NP_000199.2:p.Phe1283=
NM_001079817.1:c.3813C>T	NP_001073285.1:p.Phe1271=
NM_001079817.2:c.3813C>T	NP_001073285.1:p.Phe1271=
XM_011527988.1:c.3924C>T	XP_011526290.1:p.Phe1308=
XM_011527989.1:c.3888C>T	XP_011526291.1:p.Phe1296=
XM_011527988.2:c.3846C>T	XP_011526290.2:p.Phe1282=
XM_011527989.3:c.3810C>T	XP_011526291.2:p.Phe1270=
NM_000208.4:c.3849C>T MANE Select	NP_000199.2:p.Phe1283=
NM_001079817.3:c.3813C>T	NP_001073285.1:p.Phe1271=