Canonical Allele Identifier: CA2320769482

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128933G= , CM000681.2:g.7128933G=	GRCh38
NC_000019.9:g.7128944G= , CM000681.1:g.7128944G=	GRCh37
NC_000019.8:g.7079944G=	NCBI36
NG_008852.2:g.170068C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2864C= MANE Select	ENSP00000303830.4:p.Ala955=
ENST00000302850.9:c.2864C=	ENSP00000303830.4:p.Ala955=
ENST00000341500.9:c.2828C=	ENSP00000342838.4:p.Ala943=
NM_000208.2:c.2864C=	NP_000199.2:p.Ala955=
NM_000208.3:c.2864C=	NP_000199.2:p.Ala955=
NM_001079817.1:c.2828C=	NP_001073285.1:p.Ala943=
NM_001079817.2:c.2828C=	NP_001073285.1:p.Ala943=
XM_011527988.1:c.2939C=	XP_011526290.1:p.Ala980=
XM_011527989.1:c.2903C=	XP_011526291.1:p.Ala968=
XM_011527988.2:c.2861C=	XP_011526290.2:p.Ala954=
XM_011527989.3:c.2825C=	XP_011526291.2:p.Ala942=
NM_000208.4:c.2864C= MANE Select	NP_000199.2:p.Ala955=
NM_001079817.3:c.2828C=	NP_001073285.1:p.Ala943=