Canonical Allele Identifier: CA2320767985

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125487C= , CM000681.2:g.7125487C=	GRCh38
NC_000019.9:g.7125498C= , CM000681.1:g.7125498C=	GRCh37
NC_000019.8:g.7076498C=	NCBI36
NG_008852.2:g.173514G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3054G= MANE Select	ENSP00000303830.4:p.Val1018=
ENST00000302850.9:c.3054G=	ENSP00000303830.4:p.Val1018=
ENST00000341500.9:c.3018G=	ENSP00000342838.4:p.Val1006=
NM_000208.2:c.3054G=	NP_000199.2:p.Val1018=
NM_000208.3:c.3054G=	NP_000199.2:p.Val1018=
NM_001079817.1:c.3018G=	NP_001073285.1:p.Val1006=
NM_001079817.2:c.3018G=	NP_001073285.1:p.Val1006=
XM_011527988.1:c.3129G=	XP_011526290.1:p.Val1043=
XM_011527989.1:c.3093G=	XP_011526291.1:p.Val1031=
XM_011527988.2:c.3051G=	XP_011526290.2:p.Val1017=
XM_011527989.3:c.3015G=	XP_011526291.2:p.Val1005=
NM_000208.4:c.3054G= MANE Select	NP_000199.2:p.Val1018=
NM_001079817.3:c.3018G=	NP_001073285.1:p.Val1006=