Canonical Allele Identifier: CA2320767959

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125427A= , CM000681.2:g.7125427A=	GRCh38
NC_000019.9:g.7125438A= , CM000681.1:g.7125438A=	GRCh37
NC_000019.8:g.7076438A=	NCBI36
NG_008852.2:g.173574T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3114T= MANE Select	ENSP00000303830.4:p.Tyr1038=
ENST00000302850.9:c.3114T=	ENSP00000303830.4:p.Tyr1038=
ENST00000341500.9:c.3078T=	ENSP00000342838.4:p.Tyr1026=
NM_000208.2:c.3114T=	NP_000199.2:p.Tyr1038=
NM_000208.3:c.3114T=	NP_000199.2:p.Tyr1038=
NM_001079817.1:c.3078T=	NP_001073285.1:p.Tyr1026=
NM_001079817.2:c.3078T=	NP_001073285.1:p.Tyr1026=
XM_011527988.1:c.3189T=	XP_011526290.1:p.Tyr1063=
XM_011527989.1:c.3153T=	XP_011526291.1:p.Tyr1051=
XM_011527988.2:c.3111T=	XP_011526290.2:p.Tyr1037=
XM_011527989.3:c.3075T=	XP_011526291.2:p.Tyr1025=
NM_000208.4:c.3114T= MANE Select	NP_000199.2:p.Tyr1038=
NM_001079817.3:c.3078T=	NP_001073285.1:p.Tyr1026=