Canonical Allele Identifier: CA2320765503

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120613A= , CM000681.2:g.7120613A=	GRCh38
NC_000019.9:g.7120624A= , CM000681.1:g.7120624A=	GRCh37
NC_000019.8:g.7071624A=	NCBI36
NG_008852.2:g.178388T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3659+7T= MANE Select	ENSP00000303830.4:n.3659+7T=
ENST00000302850.9:c.3659+7T=	ENSP00000303830.4:n.3659+7T=
ENST00000341500.9:c.3623+7T=	ENSP00000342838.4:n.3623+7T=
NM_000208.2:c.3659+7T=	NP_000199.2:n.3659+7T=
NM_000208.3:c.3659+7T=	NP_000199.2:n.3659+7T=
NM_001079817.1:c.3623+7T=	NP_001073285.1:n.3623+7T=
NM_001079817.2:c.3623+7T=	NP_001073285.1:n.3623+7T=
XM_011527988.1:c.3734+7T=	XP_011526290.1:n.3734+7T=
XM_011527989.1:c.3698+7T=	XP_011526291.1:n.3698+7T=
XM_011527988.2:c.3656+7T=	XP_011526290.2:n.3656+7T=
XM_011527989.3:c.3620+7T=	XP_011526291.2:n.3620+7T=
NM_000208.4:c.3659+7T= MANE Select	NP_000199.2:n.3659+7T=
NM_001079817.3:c.3623+7T=	NP_001073285.1:n.3623+7T=