Canonical Allele Identifier: CA2320771056

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132178T= , CM000681.2:g.7132178T=	GRCh38
NC_000019.9:g.7132189T= , CM000681.1:g.7132189T=	GRCh37
NC_000019.8:g.7083189T=	NCBI36
NG_008852.2:g.166823A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2822A= MANE Select	ENSP00000303830.4:p.Tyr941=
ENST00000302850.9:c.2822A=	ENSP00000303830.4:p.Tyr941=
ENST00000341500.9:c.2786A=	ENSP00000342838.4:p.Tyr929=
NM_000208.2:c.2822A=	NP_000199.2:p.Tyr941=
NM_000208.3:c.2822A=	NP_000199.2:p.Tyr941=
NM_001079817.1:c.2786A=	NP_001073285.1:p.Tyr929=
NM_001079817.2:c.2786A=	NP_001073285.1:p.Tyr929=
XM_011527988.1:c.2900A=	XP_011526290.1:p.Tyr967=
XM_011527989.1:c.2864A=	XP_011526291.1:p.Tyr955=
XM_011527988.2:c.2822A=	XP_011526290.2:p.Tyr941=
XM_011527989.3:c.2786A=	XP_011526291.2:p.Tyr929=
NM_000208.4:c.2822A= MANE Select	NP_000199.2:p.Tyr941=
NM_001079817.3:c.2786A=	NP_001073285.1:p.Tyr929=