Canonical Allele Identifier: CA2320788151

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166032T= , CM000681.2:g.7166032T=	GRCh38
NC_000019.9:g.7166043T= , CM000681.1:g.7166043T=	GRCh37
NC_000019.8:g.7117043T=	NCBI36
NG_008852.2:g.132969A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1861+122A= MANE Select	ENSP00000303830.4:n.1861+122A=
ENST00000302850.9:c.1861+122A=	ENSP00000303830.4:n.1861+122A=
ENST00000341500.9:c.1861+122A=	ENSP00000342838.4:n.1861+122A=
ENST00000598216.1:n.1836+122A=
ENST00000600492.1:c.262+122A=	ENSP00000473170.1:n.262+122A=
NM_000208.2:c.1861+122A=	NP_000199.2:n.1861+122A=
NM_000208.3:c.1861+122A=	NP_000199.2:n.1861+122A=
NM_001079817.1:c.1861+122A=	NP_001073285.1:n.1861+122A=
NM_001079817.2:c.1861+122A=	NP_001073285.1:n.1861+122A=
XM_011527988.1:c.1939+122A=	XP_011526290.1:n.1939+122A=
XM_011527989.1:c.1939+122A=	XP_011526291.1:n.1939+122A=
XM_011527988.2:c.1861+122A=	XP_011526290.2:n.1861+122A=
XM_011527989.3:c.1861+122A=	XP_011526291.2:n.1861+122A=
NM_000208.4:c.1861+122A= MANE Select	NP_000199.2:n.1861+122A=
NM_001079817.3:c.1861+122A=	NP_001073285.1:n.1861+122A=