Canonical Allele Identifier: CA2320763833

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116967T= , CM000681.2:g.7116967T=	GRCh38
NC_000019.9:g.7116978T= , CM000681.1:g.7116978T=	GRCh37
NC_000019.8:g.7067978T=	NCBI36
NG_008852.2:g.182034A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*89A= MANE Select	ENSP00000303830.4:n.*89A=
ENST00000302850.9:c.*89A=	ENSP00000303830.4:n.*89A=
ENST00000341500.9:c.*89A=	ENSP00000342838.4:n.*89A=
NM_000208.2:c.*89A=	NP_000199.2:n.*89A=
NM_000208.3:c.*89A=	NP_000199.2:n.*89A=
NM_001079817.1:c.*89A=	NP_001073285.1:n.*89A=
NM_001079817.2:c.*89A=	NP_001073285.1:n.*89A=
XM_011527988.1:c.*89A=	XP_011526290.1:n.*89A=
XM_011527989.1:c.*89A=	XP_011526291.1:n.*89A=
XM_011527988.2:c.*89A=	XP_011526290.2:n.*89A=
XM_011527989.3:c.*89A=	XP_011526291.2:n.*89A=
NM_000208.4:c.*89A= MANE Select	NP_000199.2:n.*89A=
NM_001079817.3:c.*89A=	NP_001073285.1:n.*89A=