Canonical Allele Identifier: CA2320766501

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122927A= , CM000681.2:g.7122927A=	GRCh38
NC_000019.9:g.7122938A= , CM000681.1:g.7122938A=	GRCh37
NC_000019.8:g.7073938A=	NCBI36
NG_008852.2:g.176074T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3321T= MANE Select	ENSP00000303830.4:p.Ala1107=
ENST00000302850.9:c.3321T=	ENSP00000303830.4:p.Ala1107=
ENST00000341500.9:c.3285T=	ENSP00000342838.4:p.Ala1095=
ENST00000593970.1:n.167T=
ENST00000601099.1:n.232T=
NM_000208.2:c.3321T=	NP_000199.2:p.Ala1107=
NM_000208.3:c.3321T=	NP_000199.2:p.Ala1107=
NM_001079817.1:c.3285T=	NP_001073285.1:p.Ala1095=
NM_001079817.2:c.3285T=	NP_001073285.1:p.Ala1095=
XM_011527988.1:c.3396T=	XP_011526290.1:p.Ala1132=
XM_011527989.1:c.3360T=	XP_011526291.1:p.Ala1120=
XM_011527988.2:c.3318T=	XP_011526290.2:p.Ala1106=
XM_011527989.3:c.3282T=	XP_011526291.2:p.Ala1094=
NM_000208.4:c.3321T= MANE Select	NP_000199.2:p.Ala1107=
NM_001079817.3:c.3285T=	NP_001073285.1:p.Ala1095=