Canonical Allele Identifier: CA2320763778

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117325G= , CM000681.2:g.7117325G=	GRCh38
NC_000019.9:g.7117336G= , CM000681.1:g.7117336G=	GRCh37
NC_000019.8:g.7068336G=	NCBI36
NG_008852.2:g.181676C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3880C= MANE Select	ENSP00000303830.4:p.Leu1294=
ENST00000302850.9:c.3880C=	ENSP00000303830.4:p.Leu1294=
ENST00000341500.9:c.3844C=	ENSP00000342838.4:p.Leu1282=
NM_000208.2:c.3880C=	NP_000199.2:p.Leu1294=
NM_000208.3:c.3880C=	NP_000199.2:p.Leu1294=
NM_001079817.1:c.3844C=	NP_001073285.1:p.Leu1282=
NM_001079817.2:c.3844C=	NP_001073285.1:p.Leu1282=
XM_011527988.1:c.3955C=	XP_011526290.1:p.Leu1319=
XM_011527989.1:c.3919C=	XP_011526291.1:p.Leu1307=
XM_011527988.2:c.3877C=	XP_011526290.2:p.Leu1293=
XM_011527989.3:c.3841C=	XP_011526291.2:p.Leu1281=
NM_000208.4:c.3880C= MANE Select	NP_000199.2:p.Leu1294=
NM_001079817.3:c.3844C=	NP_001073285.1:p.Leu1282=