Canonical Allele Identifier: CA403668589

Gene: INSR

Linked Data

• COSMIC: COSM245040 ; COSM3541167
• MyVariant Identifiers: chr19:g.7117251T>C (hg19) ; chr19:g.7117240T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117240T>C , CM000681.2:g.7117240T>C	GRCh38
NC_000019.9:g.7117251T>C , CM000681.1:g.7117251T>C	GRCh37
NC_000019.8:g.7068251T>C	NCBI36
NG_008852.2:g.181761A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3965A>G MANE Select	ENSP00000303830.4:p.Glu1322Gly
ENST00000302850.9:c.3965A>G	ENSP00000303830.4:p.Glu1322Gly
ENST00000341500.9:c.3929A>G	ENSP00000342838.4:p.Glu1310Gly
NM_000208.2:c.3965A>G	NP_000199.2:p.Glu1322Gly
NM_000208.3:c.3965A>G	NP_000199.2:p.Glu1322Gly
NM_001079817.1:c.3929A>G	NP_001073285.1:p.Glu1310Gly
NM_001079817.2:c.3929A>G	NP_001073285.1:p.Glu1310Gly
XM_011527988.1:c.4040A>G	XP_011526290.1:p.Glu1347Gly
XM_011527989.1:c.4004A>G	XP_011526291.1:p.Glu1335Gly
XM_011527988.2:c.3962A>G	XP_011526290.2:p.Glu1321Gly
XM_011527989.3:c.3926A>G	XP_011526291.2:p.Glu1309Gly
NM_000208.4:c.3965A>G MANE Select	NP_000199.2:p.Glu1322Gly
NM_001079817.3:c.3929A>G	NP_001073285.1:p.Glu1310Gly