Canonical Allele Identifier: CA2320767994

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125507C= , CM000681.2:g.7125507C=	GRCh38
NC_000019.9:g.7125518C= , CM000681.1:g.7125518C=	GRCh37
NC_000019.8:g.7076518C=	NCBI36
NG_008852.2:g.173494G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3034G= MANE Select	ENSP00000303830.4:p.Val1012=
ENST00000302850.9:c.3034G=	ENSP00000303830.4:p.Val1012=
ENST00000341500.9:c.2998G=	ENSP00000342838.4:p.Val1000=
NM_000208.2:c.3034G=	NP_000199.2:p.Val1012=
NM_000208.3:c.3034G=	NP_000199.2:p.Val1012=
NM_001079817.1:c.2998G=	NP_001073285.1:p.Val1000=
NM_001079817.2:c.2998G=	NP_001073285.1:p.Val1000=
XM_011527988.1:c.3109G=	XP_011526290.1:p.Val1037=
XM_011527989.1:c.3073G=	XP_011526291.1:p.Val1025=
XM_011527988.2:c.3031G=	XP_011526290.2:p.Val1011=
XM_011527989.3:c.2995G=	XP_011526291.2:p.Val999=
NM_000208.4:c.3034G= MANE Select	NP_000199.2:p.Val1012=
NM_001079817.3:c.2998G=	NP_001073285.1:p.Val1000=