Canonical Allele Identifier: CA2320769475

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128920G= , CM000681.2:g.7128920G=	GRCh38
NC_000019.9:g.7128931G= , CM000681.1:g.7128931G=	GRCh37
NC_000019.8:g.7079931G=	NCBI36
NG_008852.2:g.170081C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2877C= MANE Select	ENSP00000303830.4:p.Ile959=
ENST00000302850.9:c.2877C=	ENSP00000303830.4:p.Ile959=
ENST00000341500.9:c.2841C=	ENSP00000342838.4:p.Ile947=
NM_000208.2:c.2877C=	NP_000199.2:p.Ile959=
NM_000208.3:c.2877C=	NP_000199.2:p.Ile959=
NM_001079817.1:c.2841C=	NP_001073285.1:p.Ile947=
NM_001079817.2:c.2841C=	NP_001073285.1:p.Ile947=
XM_011527988.1:c.2952C=	XP_011526290.1:p.Ile984=
XM_011527989.1:c.2916C=	XP_011526291.1:p.Ile972=
XM_011527988.2:c.2874C=	XP_011526290.2:p.Ile958=
XM_011527989.3:c.2838C=	XP_011526291.2:p.Ile946=
NM_000208.4:c.2877C= MANE Select	NP_000199.2:p.Ile959=
NM_001079817.3:c.2841C=	NP_001073285.1:p.Ile947=