Canonical Allele Identifier: CA2320767948

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125386G= , CM000681.2:g.7125386G=	GRCh38
NC_000019.9:g.7125397G= , CM000681.1:g.7125397G=	GRCh37
NC_000019.8:g.7076397G=	NCBI36
NG_008852.2:g.173615C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3155C= MANE Select	ENSP00000303830.4:p.Thr1052=
ENST00000302850.9:c.3155C=	ENSP00000303830.4:p.Thr1052=
ENST00000341500.9:c.3119C=	ENSP00000342838.4:p.Thr1040=
ENST00000593970.1:n.1C=
NM_000208.2:c.3155C=	NP_000199.2:p.Thr1052=
NM_000208.3:c.3155C=	NP_000199.2:p.Thr1052=
NM_001079817.1:c.3119C=	NP_001073285.1:p.Thr1040=
NM_001079817.2:c.3119C=	NP_001073285.1:p.Thr1040=
XM_011527988.1:c.3230C=	XP_011526290.1:p.Thr1077=
XM_011527989.1:c.3194C=	XP_011526291.1:p.Thr1065=
XM_011527988.2:c.3152C=	XP_011526290.2:p.Thr1051=
XM_011527989.3:c.3116C=	XP_011526291.2:p.Thr1039=
NM_000208.4:c.3155C= MANE Select	NP_000199.2:p.Thr1052=
NM_001079817.3:c.3119C=	NP_001073285.1:p.Thr1040=