Canonical Allele Identifier: CA2320766558

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7123049C= , CM000681.2:g.7123049C=	GRCh38
NC_000019.9:g.7123060C= , CM000681.1:g.7123060C=	GRCh37
NC_000019.8:g.7074060C=	NCBI36
NG_008852.2:g.175952G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3259-60G= MANE Select	ENSP00000303830.4:n.3259-60G=
ENST00000302850.9:c.3259-60G=	ENSP00000303830.4:n.3259-60G=
ENST00000341500.9:c.3223-60G=	ENSP00000342838.4:n.3223-60G=
ENST00000593970.1:n.105-60G=
ENST00000601099.1:n.110G=
NM_000208.2:c.3259-60G=	NP_000199.2:n.3259-60G=
NM_000208.3:c.3259-60G=	NP_000199.2:n.3259-60G=
NM_001079817.1:c.3223-60G=	NP_001073285.1:n.3223-60G=
NM_001079817.2:c.3223-60G=	NP_001073285.1:n.3223-60G=
XM_011527988.1:c.3334-60G=	XP_011526290.1:n.3334-60G=
XM_011527989.1:c.3298-60G=	XP_011526291.1:n.3298-60G=
XM_011527988.2:c.3256-60G=	XP_011526290.2:n.3256-60G=
XM_011527989.3:c.3220-60G=	XP_011526291.2:n.3220-60G=
NM_000208.4:c.3259-60G= MANE Select	NP_000199.2:n.3259-60G=
NM_001079817.3:c.3223-60G=	NP_001073285.1:n.3223-60G=