Canonical Allele Identifier: CA2320781047

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152862G= , CM000681.2:g.7152862G=	GRCh38
NC_000019.9:g.7152873G= , CM000681.1:g.7152873G=	GRCh37
NC_000019.8:g.7103873G=	NCBI36
NG_008852.2:g.146139C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2095C= MANE Select	ENSP00000303830.4:p.Gln699=
ENST00000302850.9:c.2095C=	ENSP00000303830.4:p.Gln699=
ENST00000341500.9:c.2095C=	ENSP00000342838.4:p.Gln699=
ENST00000598216.1:n.2070C=
NM_000208.2:c.2095C=	NP_000199.2:p.Gln699=
NM_000208.3:c.2095C=	NP_000199.2:p.Gln699=
NM_001079817.1:c.2095C=	NP_001073285.1:p.Gln699=
NM_001079817.2:c.2095C=	NP_001073285.1:p.Gln699=
XM_011527988.1:c.2173C=	XP_011526290.1:p.Gln725=
XM_011527989.1:c.2173C=	XP_011526291.1:p.Gln725=
XM_011527988.2:c.2095C=	XP_011526290.2:p.Gln699=
XM_011527989.3:c.2095C=	XP_011526291.2:p.Gln699=
NM_000208.4:c.2095C= MANE Select	NP_000199.2:p.Gln699=
NM_001079817.3:c.2095C=	NP_001073285.1:p.Gln699=