Canonical Allele Identifier: CA2320767999

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125522G= , CM000681.2:g.7125522G=	GRCh38
NC_000019.9:g.7125533G= , CM000681.1:g.7125533G=	GRCh37
NC_000019.8:g.7076533G=	NCBI36
NG_008852.2:g.173479C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3019C= MANE Select	ENSP00000303830.4:p.Pro1007=
ENST00000302850.9:c.3019C=	ENSP00000303830.4:p.Pro1007=
ENST00000341500.9:c.2983C=	ENSP00000342838.4:p.Pro995=
NM_000208.2:c.3019C=	NP_000199.2:p.Pro1007=
NM_000208.3:c.3019C=	NP_000199.2:p.Pro1007=
NM_001079817.1:c.2983C=	NP_001073285.1:p.Pro995=
NM_001079817.2:c.2983C=	NP_001073285.1:p.Pro995=
XM_011527988.1:c.3094C=	XP_011526290.1:p.Pro1032=
XM_011527989.1:c.3058C=	XP_011526291.1:p.Pro1020=
XM_011527988.2:c.3016C=	XP_011526290.2:p.Pro1006=
XM_011527989.3:c.2980C=	XP_011526291.2:p.Pro994=
NM_000208.4:c.3019C= MANE Select	NP_000199.2:p.Pro1007=
NM_001079817.3:c.2983C=	NP_001073285.1:p.Pro995=