Canonical Allele Identifier: CA403668837

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117359A>C (hg19) ; chr19:g.7117348A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117348A>C , CM000681.2:g.7117348A>C	GRCh38
NC_000019.9:g.7117359A>C , CM000681.1:g.7117359A>C	GRCh37
NC_000019.8:g.7068359A>C	NCBI36
NG_008852.2:g.181653T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3857T>G MANE Select	ENSP00000303830.4:p.Ile1286Ser
ENST00000302850.9:c.3857T>G	ENSP00000303830.4:p.Ile1286Ser
ENST00000341500.9:c.3821T>G	ENSP00000342838.4:p.Ile1274Ser
NM_000208.2:c.3857T>G	NP_000199.2:p.Ile1286Ser
NM_000208.3:c.3857T>G	NP_000199.2:p.Ile1286Ser
NM_001079817.1:c.3821T>G	NP_001073285.1:p.Ile1274Ser
NM_001079817.2:c.3821T>G	NP_001073285.1:p.Ile1274Ser
XM_011527988.1:c.3932T>G	XP_011526290.1:p.Ile1311Ser
XM_011527989.1:c.3896T>G	XP_011526291.1:p.Ile1299Ser
XM_011527988.2:c.3854T>G	XP_011526290.2:p.Ile1285Ser
XM_011527989.3:c.3818T>G	XP_011526291.2:p.Ile1273Ser
NM_000208.4:c.3857T>G MANE Select	NP_000199.2:p.Ile1286Ser
NM_001079817.3:c.3821T>G	NP_001073285.1:p.Ile1274Ser