Canonical Allele Identifier: CA2320765537

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120707C= , CM000681.2:g.7120707C=	GRCh38
NC_000019.9:g.7120718C= , CM000681.1:g.7120718C=	GRCh37
NC_000019.8:g.7071718C=	NCBI36
NG_008852.2:g.178294G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.3572G= MANE Select	NP_000199.2:p.Arg1191=
ENST00000302850.10:c.3572G= MANE Select	ENSP00000303830.4:p.Arg1191=
NM_000208.2:c.3572G=	NP_000199.2:p.Arg1191=
NM_000208.3:c.3572G=	NP_000199.2:p.Arg1191=
NM_001079817.1:c.3536G=	NP_001073285.1:p.Arg1179=
NM_001079817.2:c.3536G=	NP_001073285.1:p.Arg1179=
NM_001079817.3:c.3536G=	NP_001073285.1:p.Arg1179=
ENST00000302850.9:c.3572G=	ENSP00000303830.4:p.Arg1191=
ENST00000341500.9:c.3536G=	ENSP00000342838.4:p.Arg1179=
ENST00000601099.1:n.483G=
XM_011527988.1:c.3647G=	XP_011526290.1:p.Arg1216=
XM_011527988.2:c.3569G=	XP_011526290.2:p.Arg1190=
XM_011527989.1:c.3611G=	XP_011526291.1:p.Arg1204=
XM_011527989.3:c.3533G=	XP_011526291.2:p.Arg1178=