Canonical Allele Identifier: CA2320766378

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122658G= , CM000681.2:g.7122658G=	GRCh38
NC_000019.9:g.7122669G= , CM000681.1:g.7122669G=	GRCh37
NC_000019.8:g.7073669G=	NCBI36
NG_008852.2:g.176343C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.3485C= MANE Select	NP_000199.2:p.Ala1162=
ENST00000302850.10:c.3485C= MANE Select	ENSP00000303830.4:p.Ala1162=
NM_000208.2:c.3485C=	NP_000199.2:p.Ala1162=
NM_000208.3:c.3485C=	NP_000199.2:p.Ala1162=
NM_001079817.1:c.3449C=	NP_001073285.1:p.Ala1150=
NM_001079817.2:c.3449C=	NP_001073285.1:p.Ala1150=
NM_001079817.3:c.3449C=	NP_001073285.1:p.Ala1150=
ENST00000302850.9:c.3485C=	ENSP00000303830.4:p.Ala1162=
ENST00000341500.9:c.3449C=	ENSP00000342838.4:p.Ala1150=
ENST00000593970.1:n.331C=
ENST00000601099.1:n.396C=
XM_011527988.1:c.3560C=	XP_011526290.1:p.Ala1187=
XM_011527988.2:c.3482C=	XP_011526290.2:p.Ala1161=
XM_011527989.1:c.3524C=	XP_011526291.1:p.Ala1175=
XM_011527989.3:c.3446C=	XP_011526291.2:p.Ala1149=