Canonical Allele Identifier: CA2320766509

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122944C= , CM000681.2:g.7122944C=	GRCh38
NC_000019.9:g.7122955C= , CM000681.1:g.7122955C=	GRCh37
NC_000019.8:g.7073955C=	NCBI36
NG_008852.2:g.176057G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3304G= MANE Select	ENSP00000303830.4:p.Val1102=
ENST00000302850.9:c.3304G=	ENSP00000303830.4:p.Val1102=
ENST00000341500.9:c.3268G=	ENSP00000342838.4:p.Val1090=
ENST00000593970.1:n.150G=
ENST00000601099.1:n.215G=
NM_000208.2:c.3304G=	NP_000199.2:p.Val1102=
NM_000208.3:c.3304G=	NP_000199.2:p.Val1102=
NM_001079817.1:c.3268G=	NP_001073285.1:p.Val1090=
NM_001079817.2:c.3268G=	NP_001073285.1:p.Val1090=
XM_011527988.1:c.3379G=	XP_011526290.1:p.Val1127=
XM_011527989.1:c.3343G=	XP_011526291.1:p.Val1115=
XM_011527988.2:c.3301G=	XP_011526290.2:p.Val1101=
XM_011527989.3:c.3265G=	XP_011526291.2:p.Val1089=
NM_000208.4:c.3304G= MANE Select	NP_000199.2:p.Val1102=
NM_001079817.3:c.3268G=	NP_001073285.1:p.Val1090=