Canonical Allele Identifier: CA403668729

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117309A>C (hg19) ; chr19:g.7117298A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117298A>C , CM000681.2:g.7117298A>C	GRCh38
NC_000019.9:g.7117309A>C , CM000681.1:g.7117309A>C	GRCh37
NC_000019.8:g.7068309A>C	NCBI36
NG_008852.2:g.181703T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3907T>G MANE Select	ENSP00000303830.4:p.Phe1303Val
ENST00000302850.9:c.3907T>G	ENSP00000303830.4:p.Phe1303Val
ENST00000341500.9:c.3871T>G	ENSP00000342838.4:p.Phe1291Val
NM_000208.2:c.3907T>G	NP_000199.2:p.Phe1303Val
NM_000208.3:c.3907T>G	NP_000199.2:p.Phe1303Val
NM_001079817.1:c.3871T>G	NP_001073285.1:p.Phe1291Val
NM_001079817.2:c.3871T>G	NP_001073285.1:p.Phe1291Val
XM_011527988.1:c.3982T>G	XP_011526290.1:p.Phe1328Val
XM_011527989.1:c.3946T>G	XP_011526291.1:p.Phe1316Val
XM_011527988.2:c.3904T>G	XP_011526290.2:p.Phe1302Val
XM_011527989.3:c.3868T>G	XP_011526291.2:p.Phe1290Val
NM_000208.4:c.3907T>G MANE Select	NP_000199.2:p.Phe1303Val
NM_001079817.3:c.3871T>G	NP_001073285.1:p.Phe1291Val