Canonical Allele Identifier: CA2320771094

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132264C= , CM000681.2:g.7132264C=	GRCh38
NC_000019.9:g.7132275C= , CM000681.1:g.7132275C=	GRCh37
NC_000019.8:g.7083275C=	NCBI36
NG_008852.2:g.166737G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2736G= MANE Select	ENSP00000303830.4:p.Arg912=
ENST00000302850.9:c.2736G=	ENSP00000303830.4:p.Arg912=
ENST00000341500.9:c.2700G=	ENSP00000342838.4:p.Arg900=
NM_000208.2:c.2736G=	NP_000199.2:p.Arg912=
NM_000208.3:c.2736G=	NP_000199.2:p.Arg912=
NM_001079817.1:c.2700G=	NP_001073285.1:p.Arg900=
NM_001079817.2:c.2700G=	NP_001073285.1:p.Arg900=
XM_011527988.1:c.2814G=	XP_011526290.1:p.Arg938=
XM_011527989.1:c.2778G=	XP_011526291.1:p.Arg926=
XM_011527988.2:c.2736G=	XP_011526290.2:p.Arg912=
XM_011527989.3:c.2700G=	XP_011526291.2:p.Arg900=
NM_000208.4:c.2736G= MANE Select	NP_000199.2:p.Arg912=
NM_001079817.3:c.2700G=	NP_001073285.1:p.Arg900=