Canonical Allele Identifier: CA2320771055

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132174G= , CM000681.2:g.7132174G=	GRCh38
NC_000019.9:g.7132185G= , CM000681.1:g.7132185G=	GRCh37
NC_000019.8:g.7083185G=	NCBI36
NG_008852.2:g.166827C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2826C= MANE Select	ENSP00000303830.4:p.Phe942=
ENST00000302850.9:c.2826C=	ENSP00000303830.4:p.Phe942=
ENST00000341500.9:c.2790C=	ENSP00000342838.4:p.Phe930=
NM_000208.2:c.2826C=	NP_000199.2:p.Phe942=
NM_000208.3:c.2826C=	NP_000199.2:p.Phe942=
NM_001079817.1:c.2790C=	NP_001073285.1:p.Phe930=
NM_001079817.2:c.2790C=	NP_001073285.1:p.Phe930=
XM_011527988.1:c.2904C=	XP_011526290.1:p.Phe968=
XM_011527989.1:c.2868C=	XP_011526291.1:p.Phe956=
XM_011527988.2:c.2826C=	XP_011526290.2:p.Phe942=
XM_011527989.3:c.2790C=	XP_011526291.2:p.Phe930=
NM_000208.4:c.2826C= MANE Select	NP_000199.2:p.Phe942=
NM_001079817.3:c.2790C=	NP_001073285.1:p.Phe930=