Canonical Allele Identifier: CA403668795

Gene: INSR

Linked Data

• COSMIC: COSM119778 ; COSM4947780
• MyVariant Identifiers: chr19:g.7117339C>A (hg19) ; chr19:g.7117328C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117328C>A , CM000681.2:g.7117328C>A	GRCh38
NC_000019.9:g.7117339C>A , CM000681.1:g.7117339C>A	GRCh37
NC_000019.8:g.7068339C>A	NCBI36
NG_008852.2:g.181673G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3877G>T MANE Select	ENSP00000303830.4:p.Asp1293Tyr
ENST00000302850.9:c.3877G>T	ENSP00000303830.4:p.Asp1293Tyr
ENST00000341500.9:c.3841G>T	ENSP00000342838.4:p.Asp1281Tyr
NM_000208.2:c.3877G>T	NP_000199.2:p.Asp1293Tyr
NM_000208.3:c.3877G>T	NP_000199.2:p.Asp1293Tyr
NM_001079817.1:c.3841G>T	NP_001073285.1:p.Asp1281Tyr
NM_001079817.2:c.3841G>T	NP_001073285.1:p.Asp1281Tyr
XM_011527988.1:c.3952G>T	XP_011526290.1:p.Asp1318Tyr
XM_011527989.1:c.3916G>T	XP_011526291.1:p.Asp1306Tyr
XM_011527988.2:c.3874G>T	XP_011526290.2:p.Asp1292Tyr
XM_011527989.3:c.3838G>T	XP_011526291.2:p.Asp1280Tyr
NM_000208.4:c.3877G>T MANE Select	NP_000199.2:p.Asp1293Tyr
NM_001079817.3:c.3841G>T	NP_001073285.1:p.Asp1281Tyr