Canonical Allele Identifier: CA2320767939

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125368G= , CM000681.2:g.7125368G=	GRCh38
NC_000019.9:g.7125379G= , CM000681.1:g.7125379G=	GRCh37
NC_000019.8:g.7076379G=	NCBI36
NG_008852.2:g.173633C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3173C= MANE Select	ENSP00000303830.4:p.Thr1058=
ENST00000302850.9:c.3173C=	ENSP00000303830.4:p.Thr1058=
ENST00000341500.9:c.3137C=	ENSP00000342838.4:p.Thr1046=
ENST00000593970.1:n.19C=
NM_000208.2:c.3173C=	NP_000199.2:p.Thr1058=
NM_000208.3:c.3173C=	NP_000199.2:p.Thr1058=
NM_001079817.1:c.3137C=	NP_001073285.1:p.Thr1046=
NM_001079817.2:c.3137C=	NP_001073285.1:p.Thr1046=
XM_011527988.1:c.3248C=	XP_011526290.1:p.Thr1083=
XM_011527989.1:c.3212C=	XP_011526291.1:p.Thr1071=
XM_011527988.2:c.3170C=	XP_011526290.2:p.Thr1057=
XM_011527989.3:c.3134C=	XP_011526291.2:p.Thr1045=
NM_000208.4:c.3173C= MANE Select	NP_000199.2:p.Thr1058=
NM_001079817.3:c.3137C=	NP_001073285.1:p.Thr1046=