Canonical Allele Identifier: CA2320767960

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125429A= , CM000681.2:g.7125429A=	GRCh38
NC_000019.9:g.7125440A= , CM000681.1:g.7125440A=	GRCh37
NC_000019.8:g.7076440A=	NCBI36
NG_008852.2:g.173572T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3112T= MANE Select	ENSP00000303830.4:p.Tyr1038=
ENST00000302850.9:c.3112T=	ENSP00000303830.4:p.Tyr1038=
ENST00000341500.9:c.3076T=	ENSP00000342838.4:p.Tyr1026=
NM_000208.2:c.3112T=	NP_000199.2:p.Tyr1038=
NM_000208.3:c.3112T=	NP_000199.2:p.Tyr1038=
NM_001079817.1:c.3076T=	NP_001073285.1:p.Tyr1026=
NM_001079817.2:c.3076T=	NP_001073285.1:p.Tyr1026=
XM_011527988.1:c.3187T=	XP_011526290.1:p.Tyr1063=
XM_011527989.1:c.3151T=	XP_011526291.1:p.Tyr1051=
XM_011527988.2:c.3109T=	XP_011526290.2:p.Tyr1037=
XM_011527989.3:c.3073T=	XP_011526291.2:p.Tyr1025=
NM_000208.4:c.3112T= MANE Select	NP_000199.2:p.Tyr1038=
NM_001079817.3:c.3076T=	NP_001073285.1:p.Tyr1026=