Canonical Allele Identifier: CA2320790745

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7172404A= , CM000681.2:g.7172404A=	GRCh38
NC_000019.9:g.7172415A= , CM000681.1:g.7172415A=	GRCh37
NC_000019.8:g.7123415A=	NCBI36
NG_008852.2:g.126597T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1154T= MANE Select	ENSP00000303830.4:p.Leu385=
ENST00000302850.9:c.1154T=	ENSP00000303830.4:p.Leu385=
ENST00000341500.9:c.1154T=	ENSP00000342838.4:p.Leu385=
ENST00000598216.1:n.1129T=
NM_000208.2:c.1154T=	NP_000199.2:p.Leu385=
NM_000208.3:c.1154T=	NP_000199.2:p.Leu385=
NM_001079817.1:c.1154T=	NP_001073285.1:p.Leu385=
NM_001079817.2:c.1154T=	NP_001073285.1:p.Leu385=
XM_011527988.1:c.1232T=	XP_011526290.1:p.Leu411=
XM_011527989.1:c.1232T=	XP_011526291.1:p.Leu411=
XM_011527988.2:c.1154T=	XP_011526290.2:p.Leu385=
XM_011527989.3:c.1154T=	XP_011526291.2:p.Leu385=
NM_000208.4:c.1154T= MANE Select	NP_000199.2:p.Leu385=
NM_001079817.3:c.1154T=	NP_001073285.1:p.Leu385=