Canonical Allele Identifier: CA403668221

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117081A>C (hg19) ; chr19:g.7117070A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117070A>C , CM000681.2:g.7117070A>C	GRCh38
NC_000019.9:g.7117081A>C , CM000681.1:g.7117081A>C	GRCh37
NC_000019.8:g.7068081A>C	NCBI36
NG_008852.2:g.181931T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4135T>G MANE Select	ENSP00000303830.4:p.Ser1379Ala
ENST00000302850.9:c.4135T>G	ENSP00000303830.4:p.Ser1379Ala
ENST00000341500.9:c.4099T>G	ENSP00000342838.4:p.Ser1367Ala
NM_000208.2:c.4135T>G	NP_000199.2:p.Ser1379Ala
NM_000208.3:c.4135T>G	NP_000199.2:p.Ser1379Ala
NM_001079817.1:c.4099T>G	NP_001073285.1:p.Ser1367Ala
NM_001079817.2:c.4099T>G	NP_001073285.1:p.Ser1367Ala
XM_011527988.1:c.4210T>G	XP_011526290.1:p.Ser1404Ala
XM_011527989.1:c.4174T>G	XP_011526291.1:p.Ser1392Ala
XM_011527988.2:c.4132T>G	XP_011526290.2:p.Ser1378Ala
XM_011527989.3:c.4096T>G	XP_011526291.2:p.Ser1366Ala
NM_000208.4:c.4135T>G MANE Select	NP_000199.2:p.Ser1379Ala
NM_001079817.3:c.4099T>G	NP_001073285.1:p.Ser1367Ala