Canonical Allele Identifier: CA2320764099

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117128G= , CM000681.2:g.7117128G=	GRCh38
NC_000019.9:g.7117139G= , CM000681.1:g.7117139G=	GRCh37
NC_000019.8:g.7068139G=	NCBI36
NG_008852.2:g.181873C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4077C= MANE Select	ENSP00000303830.4:p.Ile1359=
ENST00000302850.9:c.4077C=	ENSP00000303830.4:p.Ile1359=
ENST00000341500.9:c.4041C=	ENSP00000342838.4:p.Ile1347=
NM_000208.2:c.4077C=	NP_000199.2:p.Ile1359=
NM_000208.3:c.4077C=	NP_000199.2:p.Ile1359=
NM_001079817.1:c.4041C=	NP_001073285.1:p.Ile1347=
NM_001079817.2:c.4041C=	NP_001073285.1:p.Ile1347=
XM_011527988.1:c.4152C=	XP_011526290.1:p.Ile1384=
XM_011527989.1:c.4116C=	XP_011526291.1:p.Ile1372=
XM_011527988.2:c.4074C=	XP_011526290.2:p.Ile1358=
XM_011527989.3:c.4038C=	XP_011526291.2:p.Ile1346=
NM_000208.4:c.4077C= MANE Select	NP_000199.2:p.Ile1359=
NM_001079817.3:c.4041C=	NP_001073285.1:p.Ile1347=