Canonical Allele Identifier: CA2320768000

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125523A= , CM000681.2:g.7125523A=	GRCh38
NC_000019.9:g.7125534A= , CM000681.1:g.7125534A=	GRCh37
NC_000019.8:g.7076534A=	NCBI36
NG_008852.2:g.173478T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3018T= MANE Select	ENSP00000303830.4:p.Phe1006=
ENST00000302850.9:c.3018T=	ENSP00000303830.4:p.Phe1006=
ENST00000341500.9:c.2982T=	ENSP00000342838.4:p.Phe994=
NM_000208.2:c.3018T=	NP_000199.2:p.Phe1006=
NM_000208.3:c.3018T=	NP_000199.2:p.Phe1006=
NM_001079817.1:c.2982T=	NP_001073285.1:p.Phe994=
NM_001079817.2:c.2982T=	NP_001073285.1:p.Phe994=
XM_011527988.1:c.3093T=	XP_011526290.1:p.Phe1031=
XM_011527989.1:c.3057T=	XP_011526291.1:p.Phe1019=
XM_011527988.2:c.3015T=	XP_011526290.2:p.Phe1005=
XM_011527989.3:c.2979T=	XP_011526291.2:p.Phe993=
NM_000208.4:c.3018T= MANE Select	NP_000199.2:p.Phe1006=
NM_001079817.3:c.2982T=	NP_001073285.1:p.Phe994=