Canonical Allele Identifier: CA2320767995

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125508G= , CM000681.2:g.7125508G=	GRCh38
NC_000019.9:g.7125519G= , CM000681.1:g.7125519G=	GRCh37
NC_000019.8:g.7076519G=	NCBI36
NG_008852.2:g.173493C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3033C= MANE Select	ENSP00000303830.4:p.Tyr1011=
ENST00000302850.9:c.3033C=	ENSP00000303830.4:p.Tyr1011=
ENST00000341500.9:c.2997C=	ENSP00000342838.4:p.Tyr999=
NM_000208.2:c.3033C=	NP_000199.2:p.Tyr1011=
NM_000208.3:c.3033C=	NP_000199.2:p.Tyr1011=
NM_001079817.1:c.2997C=	NP_001073285.1:p.Tyr999=
NM_001079817.2:c.2997C=	NP_001073285.1:p.Tyr999=
XM_011527988.1:c.3108C=	XP_011526290.1:p.Tyr1036=
XM_011527989.1:c.3072C=	XP_011526291.1:p.Tyr1024=
XM_011527988.2:c.3030C=	XP_011526290.2:p.Tyr1010=
XM_011527989.3:c.2994C=	XP_011526291.2:p.Tyr998=
NM_000208.4:c.3033C= MANE Select	NP_000199.2:p.Tyr1011=
NM_001079817.3:c.2997C=	NP_001073285.1:p.Tyr999=