Canonical Allele Identifier: CA403668357

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117143T>G (hg19) ; chr19:g.7117132T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117132T>G , CM000681.2:g.7117132T>G	GRCh38
NC_000019.9:g.7117143T>G , CM000681.1:g.7117143T>G	GRCh37
NC_000019.8:g.7068143T>G	NCBI36
NG_008852.2:g.181869A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4073A>C MANE Select	ENSP00000303830.4:p.His1358Pro
ENST00000302850.9:c.4073A>C	ENSP00000303830.4:p.His1358Pro
ENST00000341500.9:c.4037A>C	ENSP00000342838.4:p.His1346Pro
NM_000208.2:c.4073A>C	NP_000199.2:p.His1358Pro
NM_000208.3:c.4073A>C	NP_000199.2:p.His1358Pro
NM_001079817.1:c.4037A>C	NP_001073285.1:p.His1346Pro
NM_001079817.2:c.4037A>C	NP_001073285.1:p.His1346Pro
XM_011527988.1:c.4148A>C	XP_011526290.1:p.His1383Pro
XM_011527989.1:c.4112A>C	XP_011526291.1:p.His1371Pro
XM_011527988.2:c.4070A>C	XP_011526290.2:p.His1357Pro
XM_011527989.3:c.4034A>C	XP_011526291.2:p.His1345Pro
NM_000208.4:c.4073A>C MANE Select	NP_000199.2:p.His1358Pro
NM_001079817.3:c.4037A>C	NP_001073285.1:p.His1346Pro