Canonical Allele Identifier: CA2320767917

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125323T= , CM000681.2:g.7125323T=	GRCh38
NC_000019.9:g.7125334T= , CM000681.1:g.7125334T=	GRCh37
NC_000019.8:g.7076334T=	NCBI36
NG_008852.2:g.173678A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3218A= MANE Select	ENSP00000303830.4:p.Asn1073=
ENST00000302850.9:c.3218A=	ENSP00000303830.4:p.Asn1073=
ENST00000341500.9:c.3182A=	ENSP00000342838.4:p.Asn1061=
ENST00000593970.1:n.64A=
NM_000208.2:c.3218A=	NP_000199.2:p.Asn1073=
NM_000208.3:c.3218A=	NP_000199.2:p.Asn1073=
NM_001079817.1:c.3182A=	NP_001073285.1:p.Asn1061=
NM_001079817.2:c.3182A=	NP_001073285.1:p.Asn1061=
XM_011527988.1:c.3293A=	XP_011526290.1:p.Asn1098=
XM_011527989.1:c.3257A=	XP_011526291.1:p.Asn1086=
XM_011527988.2:c.3215A=	XP_011526290.2:p.Asn1072=
XM_011527989.3:c.3179A=	XP_011526291.2:p.Asn1060=
NM_000208.4:c.3218A= MANE Select	NP_000199.2:p.Asn1073=
NM_001079817.3:c.3182A=	NP_001073285.1:p.Asn1061=