Canonical Allele Identifier: CA2320769474

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128919C= , CM000681.2:g.7128919C=	GRCh38
NC_000019.9:g.7128930C= , CM000681.1:g.7128930C=	GRCh37
NC_000019.8:g.7079930C=	NCBI36
NG_008852.2:g.170082G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2878G= MANE Select	ENSP00000303830.4:p.Gly960=
ENST00000302850.9:c.2878G=	ENSP00000303830.4:p.Gly960=
ENST00000341500.9:c.2842G=	ENSP00000342838.4:p.Gly948=
NM_000208.2:c.2878G=	NP_000199.2:p.Gly960=
NM_000208.3:c.2878G=	NP_000199.2:p.Gly960=
NM_001079817.1:c.2842G=	NP_001073285.1:p.Gly948=
NM_001079817.2:c.2842G=	NP_001073285.1:p.Gly948=
XM_011527988.1:c.2953G=	XP_011526290.1:p.Gly985=
XM_011527989.1:c.2917G=	XP_011526291.1:p.Gly973=
XM_011527988.2:c.2875G=	XP_011526290.2:p.Gly959=
XM_011527989.3:c.2839G=	XP_011526291.2:p.Gly947=
NM_000208.4:c.2878G= MANE Select	NP_000199.2:p.Gly960=
NM_001079817.3:c.2842G=	NP_001073285.1:p.Gly948=