Canonical Allele Identifier: CA2320767907

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125296G= , CM000681.2:g.7125296G=	GRCh38
NC_000019.9:g.7125307G= , CM000681.1:g.7125307G=	GRCh37
NC_000019.8:g.7076307G=	NCBI36
NG_008852.2:g.173705C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3245C= MANE Select	ENSP00000303830.4:p.Thr1082=
ENST00000302850.9:c.3245C=	ENSP00000303830.4:p.Thr1082=
ENST00000341500.9:c.3209C=	ENSP00000342838.4:p.Thr1070=
ENST00000593970.1:n.91C=
NM_000208.2:c.3245C=	NP_000199.2:p.Thr1082=
NM_000208.3:c.3245C=	NP_000199.2:p.Thr1082=
NM_001079817.1:c.3209C=	NP_001073285.1:p.Thr1070=
NM_001079817.2:c.3209C=	NP_001073285.1:p.Thr1070=
XM_011527988.1:c.3320C=	XP_011526290.1:p.Thr1107=
XM_011527989.1:c.3284C=	XP_011526291.1:p.Thr1095=
XM_011527988.2:c.3242C=	XP_011526290.2:p.Thr1081=
XM_011527989.3:c.3206C=	XP_011526291.2:p.Thr1069=
NM_000208.4:c.3245C= MANE Select	NP_000199.2:p.Thr1082=
NM_001079817.3:c.3209C=	NP_001073285.1:p.Thr1070=