Canonical Allele Identifier: CA2320767979

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125474T= , CM000681.2:g.7125474T=	GRCh38
NC_000019.9:g.7125485T= , CM000681.1:g.7125485T=	GRCh37
NC_000019.8:g.7076485T=	NCBI36
NG_008852.2:g.173527A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3067A= MANE Select	ENSP00000303830.4:p.Ile1023=
ENST00000302850.9:c.3067A=	ENSP00000303830.4:p.Ile1023=
ENST00000341500.9:c.3031A=	ENSP00000342838.4:p.Ile1011=
NM_000208.2:c.3067A=	NP_000199.2:p.Ile1023=
NM_000208.3:c.3067A=	NP_000199.2:p.Ile1023=
NM_001079817.1:c.3031A=	NP_001073285.1:p.Ile1011=
NM_001079817.2:c.3031A=	NP_001073285.1:p.Ile1011=
XM_011527988.1:c.3142A=	XP_011526290.1:p.Ile1048=
XM_011527989.1:c.3106A=	XP_011526291.1:p.Ile1036=
XM_011527988.2:c.3064A=	XP_011526290.2:p.Ile1022=
XM_011527989.3:c.3028A=	XP_011526291.2:p.Ile1010=
NM_000208.4:c.3067A= MANE Select	NP_000199.2:p.Ile1023=
NM_001079817.3:c.3031A=	NP_001073285.1:p.Ile1011=