Canonical Allele Identifier: CA2320763692

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117182C= , CM000681.2:g.7117182C=	GRCh38
NC_000019.9:g.7117193C= , CM000681.1:g.7117193C=	GRCh37
NC_000019.8:g.7068193C=	NCBI36
NG_008852.2:g.181819G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4023G= MANE Select	ENSP00000303830.4:p.Gly1341=
ENST00000302850.9:c.4023G=	ENSP00000303830.4:p.Gly1341=
ENST00000341500.9:c.3987G=	ENSP00000342838.4:p.Gly1329=
NM_000208.2:c.4023G=	NP_000199.2:p.Gly1341=
NM_000208.3:c.4023G=	NP_000199.2:p.Gly1341=
NM_001079817.1:c.3987G=	NP_001073285.1:p.Gly1329=
NM_001079817.2:c.3987G=	NP_001073285.1:p.Gly1329=
XM_011527988.1:c.4098G=	XP_011526290.1:p.Gly1366=
XM_011527989.1:c.4062G=	XP_011526291.1:p.Gly1354=
XM_011527988.2:c.4020G=	XP_011526290.2:p.Gly1340=
XM_011527989.3:c.3984G=	XP_011526291.2:p.Gly1328=
NM_000208.4:c.4023G= MANE Select	NP_000199.2:p.Gly1341=
NM_001079817.3:c.3987G=	NP_001073285.1:p.Gly1329=