Canonical Allele Identifier: CA2320765514

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120646C= , CM000681.2:g.7120646C=	GRCh38
NC_000019.9:g.7120657C= , CM000681.1:g.7120657C=	GRCh37
NC_000019.8:g.7071657C=	NCBI36
NG_008852.2:g.178355G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3633G= MANE Select	ENSP00000303830.4:p.Gly1211=
ENST00000302850.9:c.3633G=	ENSP00000303830.4:p.Gly1211=
ENST00000341500.9:c.3597G=	ENSP00000342838.4:p.Gly1199=
ENST00000601099.1:n.544G=
NM_000208.2:c.3633G=	NP_000199.2:p.Gly1211=
NM_000208.3:c.3633G=	NP_000199.2:p.Gly1211=
NM_001079817.1:c.3597G=	NP_001073285.1:p.Gly1199=
NM_001079817.2:c.3597G=	NP_001073285.1:p.Gly1199=
XM_011527988.1:c.3708G=	XP_011526290.1:p.Gly1236=
XM_011527989.1:c.3672G=	XP_011526291.1:p.Gly1224=
XM_011527988.2:c.3630G=	XP_011526290.2:p.Gly1210=
XM_011527989.3:c.3594G=	XP_011526291.2:p.Gly1198=
NM_000208.4:c.3633G= MANE Select	NP_000199.2:p.Gly1211=
NM_001079817.3:c.3597G=	NP_001073285.1:p.Gly1199=