Canonical Allele Identifier: CA2320767987

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125496C= , CM000681.2:g.7125496C=	GRCh38
NC_000019.9:g.7125507C= , CM000681.1:g.7125507C=	GRCh37
NC_000019.8:g.7076507C=	NCBI36
NG_008852.2:g.173505G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3045G= MANE Select	ENSP00000303830.4:p.Glu1015=
ENST00000302850.9:c.3045G=	ENSP00000303830.4:p.Glu1015=
ENST00000341500.9:c.3009G=	ENSP00000342838.4:p.Glu1003=
NM_000208.2:c.3045G=	NP_000199.2:p.Glu1015=
NM_000208.3:c.3045G=	NP_000199.2:p.Glu1015=
NM_001079817.1:c.3009G=	NP_001073285.1:p.Glu1003=
NM_001079817.2:c.3009G=	NP_001073285.1:p.Glu1003=
XM_011527988.1:c.3120G=	XP_011526290.1:p.Glu1040=
XM_011527989.1:c.3084G=	XP_011526291.1:p.Glu1028=
XM_011527988.2:c.3042G=	XP_011526290.2:p.Glu1014=
XM_011527989.3:c.3006G=	XP_011526291.2:p.Glu1002=
NM_000208.4:c.3045G= MANE Select	NP_000199.2:p.Glu1015=
NM_001079817.3:c.3009G=	NP_001073285.1:p.Glu1003=