Canonical Allele Identifier: CA2320767977

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125469G= , CM000681.2:g.7125469G=	GRCh38
NC_000019.9:g.7125480G= , CM000681.1:g.7125480G=	GRCh37
NC_000019.8:g.7076480G=	NCBI36
NG_008852.2:g.173532C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3072C= MANE Select	ENSP00000303830.4:p.Thr1024=
ENST00000302850.9:c.3072C=	ENSP00000303830.4:p.Thr1024=
ENST00000341500.9:c.3036C=	ENSP00000342838.4:p.Thr1012=
NM_000208.2:c.3072C=	NP_000199.2:p.Thr1024=
NM_000208.3:c.3072C=	NP_000199.2:p.Thr1024=
NM_001079817.1:c.3036C=	NP_001073285.1:p.Thr1012=
NM_001079817.2:c.3036C=	NP_001073285.1:p.Thr1012=
XM_011527988.1:c.3147C=	XP_011526290.1:p.Thr1049=
XM_011527989.1:c.3111C=	XP_011526291.1:p.Thr1037=
XM_011527988.2:c.3069C=	XP_011526290.2:p.Thr1023=
XM_011527989.3:c.3033C=	XP_011526291.2:p.Thr1011=
NM_000208.4:c.3072C= MANE Select	NP_000199.2:p.Thr1024=
NM_001079817.3:c.3036C=	NP_001073285.1:p.Thr1012=