Canonical Allele Identifier: CA2320766453

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122830G= , CM000681.2:g.7122830G=	GRCh38
NC_000019.9:g.7122841G= , CM000681.1:g.7122841G=	GRCh37
NC_000019.8:g.7073841G=	NCBI36
NG_008852.2:g.176171C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3369+49C= MANE Select	ENSP00000303830.4:n.3369+49C=
ENST00000302850.9:c.3369+49C=	ENSP00000303830.4:n.3369+49C=
ENST00000341500.9:c.3333+49C=	ENSP00000342838.4:n.3333+49C=
ENST00000593970.1:n.215+49C=
ENST00000601099.1:n.280+49C=
NM_000208.2:c.3369+49C=	NP_000199.2:n.3369+49C=
NM_000208.3:c.3369+49C=	NP_000199.2:n.3369+49C=
NM_001079817.1:c.3333+49C=	NP_001073285.1:n.3333+49C=
NM_001079817.2:c.3333+49C=	NP_001073285.1:n.3333+49C=
XM_011527988.1:c.3444+49C=	XP_011526290.1:n.3444+49C=
XM_011527989.1:c.3408+49C=	XP_011526291.1:n.3408+49C=
XM_011527988.2:c.3366+49C=	XP_011526290.2:n.3366+49C=
XM_011527989.3:c.3330+49C=	XP_011526291.2:n.3330+49C=
NM_000208.4:c.3369+49C= MANE Select	NP_000199.2:n.3369+49C=
NM_001079817.3:c.3333+49C=	NP_001073285.1:n.3333+49C=