Canonical Allele Identifier: CA403668706

Gene: INSR

Linked Data

• MyVariant Identifiers: chr19:g.7117300T>C (hg19) ; chr19:g.7117289T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117289T>C , CM000681.2:g.7117289T>C	GRCh38
NC_000019.9:g.7117300T>C , CM000681.1:g.7117300T>C	GRCh37
NC_000019.8:g.7068300T>C	NCBI36
NG_008852.2:g.181712A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3916A>G MANE Select	ENSP00000303830.4:p.Ser1306Gly
ENST00000302850.9:c.3916A>G	ENSP00000303830.4:p.Ser1306Gly
ENST00000341500.9:c.3880A>G	ENSP00000342838.4:p.Ser1294Gly
NM_000208.2:c.3916A>G	NP_000199.2:p.Ser1306Gly
NM_000208.3:c.3916A>G	NP_000199.2:p.Ser1306Gly
NM_001079817.1:c.3880A>G	NP_001073285.1:p.Ser1294Gly
NM_001079817.2:c.3880A>G	NP_001073285.1:p.Ser1294Gly
XM_011527988.1:c.3991A>G	XP_011526290.1:p.Ser1331Gly
XM_011527989.1:c.3955A>G	XP_011526291.1:p.Ser1319Gly
XM_011527988.2:c.3913A>G	XP_011526290.2:p.Ser1305Gly
XM_011527989.3:c.3877A>G	XP_011526291.2:p.Ser1293Gly
NM_000208.4:c.3916A>G MANE Select	NP_000199.2:p.Ser1306Gly
NM_001079817.3:c.3880A>G	NP_001073285.1:p.Ser1294Gly