Canonical Allele Identifier: CA2320771101

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132284C= , CM000681.2:g.7132284C=	GRCh38
NC_000019.9:g.7132295C= , CM000681.1:g.7132295C=	GRCh37
NC_000019.8:g.7083295C=	NCBI36
NG_008852.2:g.166717G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2716G= MANE Select	ENSP00000303830.4:p.Ala906=
ENST00000302850.9:c.2716G=	ENSP00000303830.4:p.Ala906=
ENST00000341500.9:c.2680G=	ENSP00000342838.4:p.Ala894=
NM_000208.2:c.2716G=	NP_000199.2:p.Ala906=
NM_000208.3:c.2716G=	NP_000199.2:p.Ala906=
NM_001079817.1:c.2680G=	NP_001073285.1:p.Ala894=
NM_001079817.2:c.2680G=	NP_001073285.1:p.Ala894=
XM_011527988.1:c.2794G=	XP_011526290.1:p.Ala932=
XM_011527989.1:c.2758G=	XP_011526291.1:p.Ala920=
XM_011527988.2:c.2716G=	XP_011526290.2:p.Ala906=
XM_011527989.3:c.2680G=	XP_011526291.2:p.Ala894=
NM_000208.4:c.2716G= MANE Select	NP_000199.2:p.Ala906=
NM_001079817.3:c.2680G=	NP_001073285.1:p.Ala894=