Canonical Allele Identifier: CA2320771086

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132249T= , CM000681.2:g.7132249T=	GRCh38
NC_000019.9:g.7132260T= , CM000681.1:g.7132260T=	GRCh37
NC_000019.8:g.7083260T=	NCBI36
NG_008852.2:g.166752A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2751A= MANE Select	ENSP00000303830.4:p.Ser917=
ENST00000302850.9:c.2751A=	ENSP00000303830.4:p.Ser917=
ENST00000341500.9:c.2715A=	ENSP00000342838.4:p.Ser905=
NM_000208.2:c.2751A=	NP_000199.2:p.Ser917=
NM_000208.3:c.2751A=	NP_000199.2:p.Ser917=
NM_001079817.1:c.2715A=	NP_001073285.1:p.Ser905=
NM_001079817.2:c.2715A=	NP_001073285.1:p.Ser905=
XM_011527988.1:c.2829A=	XP_011526290.1:p.Ser943=
XM_011527989.1:c.2793A=	XP_011526291.1:p.Ser931=
XM_011527988.2:c.2751A=	XP_011526290.2:p.Ser917=
XM_011527989.3:c.2715A=	XP_011526291.2:p.Ser905=
NM_000208.4:c.2751A= MANE Select	NP_000199.2:p.Ser917=
NM_001079817.3:c.2715A=	NP_001073285.1:p.Ser905=